- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01088503
Traitement avec des inhibiteurs des récepteurs de l'adénosine diphosphate (ADP) : évaluation longitudinale des schémas de traitement et des événements après un syndrome coronarien aigu (TRANSLATE-ACS)
L'étude TRANSLATE-ACS : Traitement avec des inhibiteurs des récepteurs de l'ADP : évaluation longitudinale des schémas de traitement et des événements après un syndrome coronarien aigu
L'étude TReatment with ADP receptor iNhibitorS: Longitudinal Assessment of Treatment Patterns and Events after Acute Coronary Syndrome (TRANSLATE-ACS) est une étude longitudinale prospective et observationnelle visant à évaluer l'efficacité et l'utilisation réelles du prasugrel et d'autres thérapies par inhibiteurs des récepteurs de l'ADP dans l'infarctus du myocarde (IM) participants traités par intervention coronarienne percutanée (ICP) pendant l'hospitalisation index. La gestion des participants et les décisions de traitement sont à la discrétion de l'équipe de soins selon la pratique clinique de routine. Environ 17 000 participants seront inscrits dans environ 350 sites aux États-Unis. Le suivi sera effectué pendant 15 mois auprès d'environ 15 650 participants.
TRANSLATE-ACS complétera les résultats des essais cliniques contrôlés randomisés et des registres actuels en abordant les schémas de traitement et les résultats cliniques du monde réel pour les participants à l'IDM gérés par ICP et initiés au traitement par inhibiteur des récepteurs de l'ADP. En plus de déterminer l'efficacité du prasugrel par rapport à d'autres inhibiteurs des récepteurs de l'ADP, l'étude déterminera également les facteurs associés à la sélection initiale des inhibiteurs des récepteurs de l'ADP et aux schémas longitudinaux d'utilisation, évaluera l'innocuité, et décrira et comparera l'utilisation des ressources et les coûts médicaux associés à Inhibiteurs des récepteurs de l'ADP. De plus, cette étude générera un continuum d'informations des patients hospitalisés aux patients externes pour fournir une image complète du traitement des participants et des résultats qui ne sont pas actuellement disponibles pour les nouveaux inhibiteurs des récepteurs de l'ADP.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
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Rio Piedras, Porto Rico, 00924
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Alabama
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Birmingham, Alabama, États-Unis, 35233
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Mobile, Alabama, États-Unis, 36617
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Alaska
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Anchorage, Alaska, États-Unis, 99508
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Fayetteville, Alaska, États-Unis, 72703
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Arizona
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Gilbert, Arizona, États-Unis, 85297
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Scottsdale, Arizona, États-Unis, 85258
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Tucson, Arizona, États-Unis, 85723
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Arkansas
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Fort Smith, Arkansas, États-Unis, 72901
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Little Rock, Arkansas, États-Unis, 72205
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Rogers, Arkansas, États-Unis, 72758
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California
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Berkeley, California, États-Unis, 94705
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Loma Linda, California, États-Unis, 92354
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Newport Beach, California, États-Unis, 92663
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Northridge, California, États-Unis, 91325
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Roseville, California, États-Unis, 95661
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Sacramento, California, États-Unis, 95819
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Salinas, California, États-Unis, 93901
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Santa Barbara, California, États-Unis, 93105
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Stockton, California, États-Unis, 95204
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Thousand Oaks, California, États-Unis, 91360
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Torrance, California, États-Unis, 90505
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Colorado
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Aurora, Colorado, États-Unis, 80045
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Parker, Colorado, États-Unis, 80138
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Connecticut
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Bridgeport, Connecticut, États-Unis, 06610
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Danbury, Connecticut, États-Unis, 06810
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Farmington, Connecticut, États-Unis, 06030
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Hartford, Connecticut, États-Unis, 06102
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Delaware
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Newark, Delaware, États-Unis, 19718
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District of Columbia
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Washington, District of Columbia, États-Unis, 20010
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Florida
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Atlantis, Florida, États-Unis, 33462
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Brandon, Florida, États-Unis, 33511
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Ft Lauderdale, Florida, États-Unis, 33308
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Gainesville, Florida, États-Unis, 32608
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Hudson, Florida, États-Unis, 34667
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Jacksonville, Florida, États-Unis, 32209
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Lakeland, Florida, États-Unis, 33805
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Melbourne, Florida, États-Unis, 32901
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Miami Beach, Florida, États-Unis, 33140
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Ocala, Florida, États-Unis, 34471
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Orlando, Florida, États-Unis, 32806
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Stuart, Florida, États-Unis, 34996
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Tampa, Florida, États-Unis, 33613
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Vero Beach, Florida, États-Unis, 32960
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Wellington, Florida, États-Unis, 33449
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Winter Haven, Florida, États-Unis, 33881
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Georgia
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Columbus, Georgia, États-Unis, 31904
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Marietta, Georgia, États-Unis, 30060
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Riverdale, Georgia, États-Unis, 30274
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Hawaii
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Honolulu, Hawaii, États-Unis, 96813
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Illinois
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Carbondale, Illinois, États-Unis, 62901
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Chicago, Illinois, États-Unis, 60625
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Geneva, Illinois, États-Unis, 60134
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Hoffman Estates, Illinois, États-Unis, 60169
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Joliet, Illinois, États-Unis, 60435
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Oak Lawn, Illinois, États-Unis, 60453
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Peoria, Illinois, États-Unis, 61614
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Rock Island, Illinois, États-Unis, 61201
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Rockford, Illinois, États-Unis, 61107
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Urbana, Illinois, États-Unis, 61801
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Indiana
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Elkhart, Indiana, États-Unis, 46514
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Ft Wayne, Indiana, États-Unis, 46805
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Hammond, Indiana, États-Unis, 46320
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Indianapolis, Indiana, États-Unis, 46250
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Lafayette, Indiana, États-Unis, 47905
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Muncie, Indiana, États-Unis, 47303
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Iowa
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Davenport, Iowa, États-Unis, 52803
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Kansas
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Kansas City, Kansas, États-Unis, 66160
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Overland Park, Kansas, États-Unis, 66209
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Topeka, Kansas, États-Unis, 66604
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Wichita, Kansas, États-Unis, 67220
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Kentucky
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Crestview Hills, Kentucky, États-Unis, 41017
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Lexington, Kentucky, États-Unis, 40504
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Owensboro, Kentucky, États-Unis, 42303
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Louisiana
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Alexandria, Louisiana, États-Unis, 71301
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Maine
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Lewiston, Maine, États-Unis, 04240
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Maryland
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Annapolis, Maryland, États-Unis, 21401
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Baltimore, Maryland, États-Unis, 21215
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Cumberland, Maryland, États-Unis, 21502
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Hagerstown, Maryland, États-Unis, 21740
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Salisbury, Maryland, États-Unis, 21804
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Takoma Park, Maryland, États-Unis, 20912
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Massachusetts
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Worcester, Massachusetts, États-Unis, 01606
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Michigan
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Ann Arbor, Michigan, États-Unis, 48109
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Bay City, Michigan, États-Unis, 48708
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Dearborn, Michigan, États-Unis, 48124
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Detroit, Michigan, États-Unis, 48202
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Flint, Michigan, États-Unis, 48532
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Grand Blanc, Michigan, États-Unis, 48439
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Marquette, Michigan, États-Unis, 49855
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Mount Clemens, Michigan, États-Unis, 48043
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Saginaw, Michigan, États-Unis, 48602
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Southfield, Michigan, États-Unis, 48075
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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St. Joseph, Michigan, États-Unis, 49085
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Troy, Michigan, États-Unis, 48085
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Warren, Michigan, États-Unis, 48093
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wyoming, Michigan, États-Unis, 49519
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Minnesota
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Coon Rapids, Minnesota, États-Unis, 55433
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Duluth, Minnesota, États-Unis, 55805
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Edina, Minnesota, États-Unis, 55435
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Minneapolis, Minnesota, États-Unis, 55455
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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St Cloud, Minnesota, États-Unis, 56303
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Missouri
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Columbia, Missouri, États-Unis, 65212
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Joplin, Missouri, États-Unis, 64804
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kansas City, Missouri, États-Unis, 64114
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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North Kansas City, Missouri, États-Unis, 64116
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Springfield, Missouri, États-Unis, 65804
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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St Louis, Missouri, États-Unis, 63141
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Montana
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Bozeman, Montana, États-Unis, 59715
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Kalispell, Montana, États-Unis, 59901
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Nebraska
-
Omaha, Nebraska, États-Unis, 68198
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Nevada
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Las Vegas, Nevada, États-Unis, 89102
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Reno, Nevada, États-Unis, 89503
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New Hampshire
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Nashua, New Hampshire, États-Unis, 03060
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New Jersey
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Bridgewater, New Jersey, États-Unis, 08807
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Cherry Hill, New Jersey, États-Unis, 08034
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New Brunswick, New Jersey, États-Unis, 08901
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Newark, New Jersey, États-Unis, 07055
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Ridgewood, New Jersey, États-Unis, 07450
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Summit, New Jersey, États-Unis, 07902
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New Mexico
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Albuquerque, New Mexico, États-Unis, 87131
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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New York
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Brooklyn, New York, États-Unis, 11215
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Elmira, New York, États-Unis, 14905
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Johnson City, New York, États-Unis, 13790
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
New York, New York, États-Unis, 10075
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Stony Brook, New York, États-Unis, 11794
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Utica, New York, États-Unis, 13501
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Valhalla, New York, États-Unis, 10595
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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North Carolina
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Chapel Hill, North Carolina, États-Unis, 27599
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lumberton, North Carolina, États-Unis, 28358
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Raleigh, North Carolina, États-Unis, 27609
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Wilmington, North Carolina, États-Unis, 28402
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Winston-Salem, North Carolina, États-Unis, 27157
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Ohio
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Canton, Ohio, États-Unis, 44710
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Cincinnati, Ohio, États-Unis, 45267
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Kettering, Ohio, États-Unis, 45429
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Middleburg Heights, Ohio, États-Unis, 44130
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Toledo, Ohio, États-Unis, 43615
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Youngstown, Ohio, États-Unis, 44501
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Oklahoma
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Oklahoma City, Oklahoma, États-Unis, 73112
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Oregon
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Bend, Oregon, États-Unis, 97701
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Portland, Oregon, États-Unis, 97225
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Tualatin, Oregon, États-Unis, 97062
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Pennsylvania
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Abington, Pennsylvania, États-Unis, 19001
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Allentown, Pennsylvania, États-Unis, 18104
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Bryn Mawr, Pennsylvania, États-Unis, 19010
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Camp Hill, Pennsylvania, États-Unis, 17011
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Danville, Pennsylvania, États-Unis, 17822
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Darby, Pennsylvania, États-Unis, 19023
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Greensburg, Pennsylvania, États-Unis, 15601
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Harrisburg, Pennsylvania, États-Unis, 17111
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Hershey, Pennsylvania, États-Unis, 17033
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Johnstown, Pennsylvania, États-Unis, 15905
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Lancaster, Pennsylvania, États-Unis, 17602
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Langhorne, Pennsylvania, États-Unis, 19047
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Philadelphia, Pennsylvania, États-Unis, 19140
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Pittsburgh, Pennsylvania, États-Unis, 15240
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Sayre, Pennsylvania, États-Unis, 18840
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Uniontown, Pennsylvania, États-Unis, 15401
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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South Carolina
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Anderson, South Carolina, États-Unis, 29621
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Charleston, South Carolina, États-Unis, 29485
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Columbia, South Carolina, États-Unis, 29203
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Tennessee
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Memphis, Tennessee, États-Unis, 38120
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
Nashville, Tennessee, États-Unis, 37205
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
-
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Texas
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Dallas, Texas, États-Unis, 75216
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Decatur, Texas, États-Unis, 76234
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Grapevine, Texas, États-Unis, 76051
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Houston, Texas, États-Unis, 77030
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Round Rock, Texas, États-Unis, 78665
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Temple, Texas, États-Unis, 76508
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Virginia
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Charlottesville, Virginia, États-Unis, 22908
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Chesapeake, Virginia, États-Unis, 23320
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Danville, Virginia, États-Unis, 24541
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Newport News, Virginia, États-Unis, 23601
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Norfolk, Virginia, États-Unis, 23507
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Richmond, Virginia, États-Unis, 23320
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Roanoke, Virginia, États-Unis, 24018
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Virginia Beach, Virginia, États-Unis, 23454
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Winchester, Virginia, États-Unis, 22601
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Washington
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Bellevue, Washington, États-Unis, 98004
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Everett, Washington, États-Unis, 98201
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West Virginia
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Huntington, West Virginia, États-Unis, 25701
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Wisconsin
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Green Bay, Wisconsin, États-Unis, 54308
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Milwaukee, Wisconsin, États-Unis, 53215
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Racine, Wisconsin, États-Unis, 53405
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Waukesha, Wisconsin, États-Unis, 53188
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Critère d'intégration:
- supérieur ou égal à 18 ans
- diagnostiqué avec NSTEMI ou STEMI traité avec une ICP pendant l'hospitalisation index
- commencé (ou poursuivi) un traitement par inhibiteur des récepteurs de l'ADP avant le congé
- pleinement informés et capables de fournir un consentement écrit pour le suivi longitudinal et la collecte de données
Critère d'exclusion:
- participer simultanément à une étude de recherche qui oriente le choix d'un inhibiteur des récepteurs de l'ADP expérimental ou approuvé dans les 12 premiers mois suivant l'IM
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
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Traitement par inhibiteur des récepteurs de l'ADP
Participants admis pour un infarctus du myocarde sans élévation du segment ST (NSTEMI) ou un infarctus du myocarde avec élévation du segment ST (STEMI) subissant une intervention coronarienne percutanée (ICP) et traités avec un inhibiteur des récepteurs de l'ADP pendant l'hospitalisation initiale.
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Schéma posologique tel que déterminé par le médecin traitant.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Pourcentage de participants présentant des événements cardiovasculaires indésirables majeurs (MACE)
Délai: Base de référence jusqu'à 12 mois
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Le MACE est défini comme un composite de décès toutes causes confondues, d'infarctus du myocarde (IM), d'accident vasculaire cérébral ou de revascularisation coronarienne non planifiée.
Les événements survenus plus de 7 jours après le changement ou l'arrêt du traitement ont été exclus de l'analyse.
Les pourcentages observés (non ajustés) de participants atteints de MACE, ainsi que les analyses statistiques ajustées pour les différences de cohorte de base, sont présentés.
Pourcentage de participants = (nombre de participants avec des événements dans 12 mois/nombre de participants traités) * 100.
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Base de référence jusqu'à 12 mois
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Facteurs associés à la sélection initiale des inhibiteurs des récepteurs de l'adénosine diphosphate (ADP) lors de l'inscription
Délai: Jour 0 (inscription à l'étude)
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Les facteurs sont le placement d'un stent à élution médicamenteuse (DES) par rapport au placement d'un stent en métal nu (BMS), autre (pas de stent) par rapport à BMS, STEMI, autre race, choc cardiogénique survenu dans les 24 heures, homme, questionnaire européen sur la qualité de vie-5 dimension Score d'état de santé (EQ-5D) - Indice des États-Unis (US) = 1 vs <1, marié, diabétique et autre par rapport au placement BMS.
L'indice EQ-5D US est un instrument de qualité de vie lié à la santé et évalué par les participants, basé sur la population américaine.
Les scores vont de -0,11 à 1,0 avec 1,0 = santé parfaite.
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Jour 0 (inscription à l'étude)
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Facteurs associés à la sélection initiale des inhibiteurs des récepteurs de l'ADP lors de l'inscription : hémoglobine avant l'intervention
Délai: Jour 0 (inscription à l'étude)
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Jour 0 (inscription à l'étude)
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Facteurs associés à la sélection initiale des inhibiteurs des récepteurs de l'ADP à l'inscription : indice de maladie coronarienne de Duke (CAD)
Délai: Jour 0 (inscription à l'étude)
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L'indice Duke CAD est une mesure composite validée de la charge angiographique, qui attribue des poids pronostiques de 1 à 100.
Des scores plus élevés indiquent une charge angiographique plus importante et sont associés à un pronostic plus sombre.
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Jour 0 (inscription à l'étude)
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
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Pourcentage de participants présentant des événements hémorragiques graves ou modérés cumulatifs
Délai: Baseline, 1, 6, 12 et 15 mois
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Les événements hémorragiques ont été recueillis à l'aide de la définition de saignement de l'utilisation globale de la streptokinase et de l'activateur tissulaire du plasminogène pour les artères coronaires occluses (GUSTO).
Une hémorragie grave ou potentiellement mortelle liée à un pontage aortocoronarien (PAC) liée à un pontage GUSTO est toute hémorragie intracrânienne OU tout événement hémorragique entraînant une atteinte hémodynamique importante nécessitant un traitement.
Le saignement modéré GUSTO non lié au PAC est tout événement hémorragique nécessitant une transfusion qui n'est pas considéré comme un saignement grave GUSTO ou mettant la vie en danger.
Les événements hémorragiques supplémentaires sont les saignements mortels ou ICH, ou tout événement hémorragique non mortel lié à la chirurgie entraînant ≥ 4 unités de transfusion de globules rouges.
Les pourcentages observés (non ajustés) de participants présentant des événements hémorragiques, ainsi que les analyses statistiques ajustées pour les différences de cohorte de base, sont présentés.
Pourcentage de participants = (nombre de participants avec événements / nombre de participants traités) * 100.
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Baseline, 1, 6, 12 et 15 mois
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Pourcentage de participants avec MACE et qui n'avaient aucun antécédent d'attaque ischémique transitoire (AIT)/AVC, pèsent ≥ 60 kilogrammes (kg) et sont âgés de moins de 75 ans
Délai: Base de référence jusqu'à 12 mois
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Le MACE est défini comme un composite de décès toutes causes confondues, d'infarctus du myocarde, d'accident vasculaire cérébral ou de revascularisation coronarienne non planifiée.
Les événements survenus plus de 7 jours après le changement ou l'arrêt du traitement ont été exclus de l'analyse.
Les pourcentages observés (non ajustés) de participants atteints de MACE, ainsi que les analyses statistiques ajustées pour les différences de cohorte de base, sont présentés.
Pourcentage de participants = (nombre de participants avec événements / nombre de participants traités) * 100.
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Base de référence jusqu'à 12 mois
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Pourcentage de participants avec MACE sur 1, 6 et 15 mois
Délai: Baseline à 1, 6 et 15 mois
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Le MACE est défini comme un composite de décès toutes causes confondues, d'infarctus du myocarde, d'accident vasculaire cérébral ou de revascularisation coronarienne non planifiée.
Les événements survenus plus de 7 jours après le changement ou l'arrêt du traitement ont été exclus de l'analyse.
Les pourcentages observés (non ajustés) de participants atteints de MACE sont présentés.
L'analyse de Kaplan-Meier a été utilisée pour estimer le pourcentage de participants avec un événement MACE.
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Baseline à 1, 6 et 15 mois
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Pourcentage de participants présentant des événements de thrombose de stent (ST) certains ou probables
Délai: Base de référence sur 15 mois
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Les critères de l'Academic Research Consortium (ARC) ont été utilisés pour définir ST.
Le ST définitif est une confirmation angiographique ou pathologique de l'occlusion thrombotique partielle ou totale dans la région péri-stent, et au moins 1 des critères supplémentaires suivants : symptômes ischémiques aigus ; modifications ischémiques de l'électrocardiogramme ; biomarqueurs cardiaques élevés.
Le ST probable est tout décès inexpliqué dans les 30 jours suivant l'implantation du stent ; tout IM, qui est lié à une ischémie aiguë documentée dans le territoire du stent implanté sans confirmation angiographique du ST et en l'absence de toute autre cause évidente.
Les événements survenus plus de 7 jours après le changement ou l'arrêt du traitement ont été exclus de l'analyse.
Les pourcentages observés (non ajustés) de participants présentant des événements ST sont présentés.
L'analyse de Kaplan-Meier a été utilisée pour estimer le pourcentage de participants avec un événement ST certain ou probable.
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Base de référence sur 15 mois
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Modèles d'utilisation des ressources, coûts médicaux totaux cumulés et rapport coût-efficacité
Délai: 15 mois
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15 mois
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Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Directeur d'études: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours EST), Eli Lilly and Company
Publications et liens utiles
Publications générales
- Rymer JA, Kaltenbach LA, Doll JA, Messenger JC, Peterson ED, Wang TY. Safety of Dual-Antiplatelet Therapy After Myocardial Infarction Among Patients With Chronic Kidney Disease. J Am Heart Assoc. 2019 May 21;8(10):e012236. doi: 10.1161/JAHA.119.012236.
- Warraich HJ, Kaltenbach LA, Fonarow GC, Peterson ED, Wang TY. Adverse Change in Employment Status After Acute Myocardial Infarction: Analysis From the TRANSLATE-ACS Study. Circ Cardiovasc Qual Outcomes. 2018 Jun;11(6):e004528. doi: 10.1161/CIRCOUTCOMES.117.004528.
- Fanaroff AC, Kaltenbach LA, Peterson ED, Akhter MW, Effron MB, Henry TD, Wang TY. Antiplatelet Therapy Changes for Patients With Myocardial Infarction With Recurrent Ischemic Events: Insights Into Contemporary Practice From the TRANSLATE-ACS (Treatment With ADP Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome) Study. J Am Heart Assoc. 2018 Feb 8;7(4):e007982. doi: 10.1161/JAHA.117.007982.
- Tisminetzky M, Wang TY, Gurwitz J, Kaltenbach LA, McManus D, Gore J, Peterson E, Goldberg RJ. Magnitude and Characteristics of Patients Who Survived an Acute Myocardial Infarction. J Am Heart Assoc. 2017 Sep 25;6(9):e006373. doi: 10.1161/JAHA.117.006373.
- Guimaraes PO, Krishnamoorthy A, Kaltenbach LA, Anstrom KJ, Effron MB, Mark DB, McCollam PL, Davidson-Ray L, Peterson ED, Wang TY. Accuracy of Medical Claims for Identifying Cardiovascular and Bleeding Events After Myocardial Infarction : A Secondary Analysis of the TRANSLATE-ACS Study. JAMA Cardiol. 2017 Jul 1;2(7):750-757. doi: 10.1001/jamacardio.2017.1460.
- Hess CN, Kaltenbach LA, Doll JA, Cohen DJ, Peterson ED, Wang TY. Race and Sex Differences in Post-Myocardial Infarction Angina Frequency and Risk of 1-Year Unplanned Rehospitalization. Circulation. 2017 Feb 7;135(6):532-543. doi: 10.1161/CIRCULATIONAHA.116.024406.
- Jackson LR 2nd, Peterson ED, McCoy LA, Ju C, Zettler M, Baker BA, Messenger JC, Faries DE, Effron MB, Cohen DJ, Wang TY. Impact of Proton Pump Inhibitor Use on the Comparative Effectiveness and Safety of Prasugrel Versus Clopidogrel: Insights From the Treatment With Adenosine Diphosphate Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome (TRANSLATE-ACS) Study. J Am Heart Assoc. 2016 Oct 21;5(10):e003824. doi: 10.1161/JAHA.116.003824.
- Fosbol EL, Ju C, Anstrom KJ, Zettler ME, Messenger JC, Waksman R, Effron MB, Baker BA, Cohen DJ, Peterson ED, Wang TY. Early Cessation of Adenosine Diphosphate Receptor Inhibitors Among Acute Myocardial Infarction Patients Treated With Percutaneous Coronary Intervention: Insights From the TRANSLATE-ACS Study (Treatment With Adenosine Diphosphate Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome). Circ Cardiovasc Interv. 2016 Nov;9(11):e003602. doi: 10.1161/CIRCINTERVENTIONS.115.003602.
- Krishnamoorthy A, Peterson ED, Knight JD, Anstrom KJ, Effron MB, Zettler ME, Davidson-Ray L, Baker BA, McCollam PL, Mark DB, Wang TY. How Reliable are Patient-Reported Rehospitalizations? Implications for the Design of Future Practical Clinical Studies. J Am Heart Assoc. 2016 Jan 25;5(1):e002695. doi: 10.1161/JAHA.115.002695.
- Hess CN, Wang TY, McCoy LA, Messenger JC, Effron MB, Zettler ME, Henry TD, Peterson ED, Fonarow GC. Unplanned Inpatient and Observation Rehospitalizations After Acute Myocardial Infarction: Insights From the Treatment With Adenosine Diphosphate Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome (TRANSLATE-ACS) Study. Circulation. 2016 Feb 2;133(5):493-501. doi: 10.1161/CIRCULATIONAHA.115.017001. Epub 2015 Dec 17.
- Wang TY, Henry TD, McCoy LA, Berger PB, Cohen DJ, Effron MB, Zettler M, Baker BA, Messenger JC, Peterson ED. Contemporary use of platelet function and pharmacogenomic testing among patients with acute myocardial infarction undergoing percutaneous coronary intervention in the United States. Am Heart J. 2015 Oct;170(4):706-14. doi: 10.1016/j.ahj.2015.06.021. Epub 2015 Jul 2.
- Mathews R, Wang TY, Honeycutt E, Henry TD, Zettler M, Chang M, Fonarow GC, Peterson ED; TRANSLATE-ACS Study Investigators. Persistence with secondary prevention medications after acute myocardial infarction: Insights from the TRANSLATE-ACS study. Am Heart J. 2015 Jul;170(1):62-9. doi: 10.1016/j.ahj.2015.03.019. Epub 2015 Apr 2.
- Mathews R, Peterson ED, Honeycutt E, Chin CT, Effron MB, Zettler M, Fonarow GC, Henry TD, Wang TY. Early Medication Nonadherence After Acute Myocardial Infarction: Insights into Actionable Opportunities From the TReatment with ADP receptor iNhibitorS: Longitudinal Assessment of Treatment Patterns and Events after Acute Coronary Syndrome (TRANSLATE-ACS) Study. Circ Cardiovasc Qual Outcomes. 2015 Jul;8(4):347-56. doi: 10.1161/CIRCOUTCOMES.114.001223. Epub 2015 Jun 2.
- Wang TY, Henry TD, Effron MB, Honeycutt E, Hess CN, Zettler ME, Cohen DJ, Baker BA, Berger PB, Anstrom KJ, Angiolillo DJ, Peterson ED; TRANSLATE-POPS Investigators. Cluster-randomized clinical trial examining the impact of platelet function testing on practice: the treatment with adenosine diphosphate receptor inhibitors: longitudinal assessment of treatment patterns and events after acute coronary syndrome prospective open label antiplatelet therapy study. Circ Cardiovasc Interv. 2015 Jun;8(6):e001712. doi: 10.1161/CIRCINTERVENTIONS.114.001712.
- Xian Y, Wang TY, McCoy LA, Effron MB, Henry TD, Bach RG, Zettler ME, Baker BA, Fonarow GC, Peterson ED. Association of Discharge Aspirin Dose With Outcomes After Acute Myocardial Infarction: Insights From the Treatment with ADP Receptor Inhibitors: Longitudinal Assessment of Treatment Patterns and Events after Acute Coronary Syndrome (TRANSLATE-ACS) Study. Circulation. 2015 Jul 21;132(3):174-81. doi: 10.1161/CIRCULATIONAHA.114.014992. Epub 2015 May 20.
- Bagai A, Peterson ED, Honeycutt E, Effron MB, Cohen DJ, Goodman SG, Anstrom KJ, Gupta A, Messenger JC, Wang TY. In-hospital switching between adenosine diphosphate receptor inhibitors in patients with acute myocardial infarction treated with percutaneous coronary intervention: Insights into contemporary practice from the TRANSLATE-ACS study. Eur Heart J Acute Cardiovasc Care. 2015 Dec;4(6):499-508. doi: 10.1177/2048872614564082. Epub 2014 Dec 16.
- Hess CN, McCoy LA, Duggirala HJ, Tavris DR, O'Callaghan K, Douglas PS, Peterson ED, Wang TY. Sex-based differences in outcomes after percutaneous coronary intervention for acute myocardial infarction: a report from TRANSLATE-ACS. J Am Heart Assoc. 2014 Feb 7;3(1):e000523. doi: 10.1161/JAHA.113.000523.
- Wang TY, McCoy L, Henry TD, Effron MB, Messenger JC, Cohen DJ, Mark DB, Stone GW, Zettler M, Singh M, Fonarow GC, Peterson ED; TRANSLATE-ACS Study Investigators. Early post-discharge bleeding and antiplatelet therapy discontinuation among acute myocardial infarction patients treated with percutaneous coronary intervention. J Am Coll Cardiol. 2014 Apr 29;63(16):1700-2. doi: 10.1016/j.jacc.2013.12.012. Epub 2014 Jan 30. No abstract available.
- Chin CT, Wang TY, Anstrom KJ, Zhu B, Maa JF, Messenger JC, Ryan KA, Davidson-Ray L, Zettler M, Effron MB, Mark DB, Peterson ED. Treatment with adenosine diphosphate receptor inhibitors-longitudinal assessment of treatment patterns and events after acute coronary syndrome (TRANSLATE-ACS) study design: expanding the paradigm of longitudinal observational research. Am Heart J. 2011 Nov;162(5):844-51. doi: 10.1016/j.ahj.2011.08.021.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 12549
- H7T-US-B007 (Autre identifiant: Eli Lilly and Company)
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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