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Effekt og sikkerhet av Drotrecogin Alfa (aktivert) hos voksne pasienter med septisk sjokk

20. august 2012 oppdatert av: Eli Lilly and Company

En randomisert, dobbeltblind, placebokontrollert, multisenter, fase 3-studie av Drotrecogin Alfa (aktivert) administrert som en kontinuerlig 96-timers infusjon til voksne pasienter med septisk sjokk

Hensikten med denne placebokontrollerte studien er å bestemme om drotrecogin alfa (aktivert) behandling gir signifikant forbedring av dødelighetsreduksjon hos pasienter med septisk sjokk sammenlignet med placebobehandling hos pasienter som mottar gjeldende standard for behandling for septisk sjokk. Denne studien vil også vurdere effektiviteten til drotrecogin alfa (aktivert) for å redusere 28-dagers dødelighet hos pasienter med septisk sjokk og samtidig alvorlig protein C-mangel.

Studieoversikt

Status

Fullført

Forhold

Studietype

Intervensjonell

Registrering (Faktiske)

1696

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Australian Capital Territory
      • Garran, Australian Capital Territory, Australia, 2605
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    • New South Wales
      • Newcastle, New South Wales, Australia, 2305
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      • St. Leonards, New South Wales, Australia, 2065
        • 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.
    • Queensland
      • Herston, Queensland, Australia, 4029
        • 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.
    • South Australia
      • Adelaide, South Australia, Australia, 5000
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    • Victoria
      • Box Hill, Victoria, Australia, 3128
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      • Epping, Victoria, Australia, 3076
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      • Heidelberg, Victoria, Australia, 3084
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      • Melbourne, Victoria, Australia, 3004
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      • Parkville, Victoria, Australia, 3050
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      • Antwerp, Belgia, 2020
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      • Antwerpen, Belgia, 2060
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      • Brussels, Belgia, 1200
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      • Edegem, Belgia, 2650
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      • Genk, Belgia, 3600
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      • Leuven, Belgia, 3000
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      • Liège, Belgia, 4000
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      • Ottignies, Belgia, 1340
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      • Roeselare, Belgia, 8800
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      • Wilrijk, Belgia, 2610
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      • Yvoir, Belgia, 5530
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      • Belo Horizonte, Brasil, 30140-093
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      • Joinville, Brasil, 89202-050
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      • Londrina, Brasil, 86038
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      • Porto Alegre, Brasil, 90610-970
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      • Sao Jose Rio Preto, Brasil, 15090
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      • São Paulo, Brasil, 05403-000
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    • Alberta
      • Calgary, Alberta, Canada, T2N 2T9
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    • British Columbia
      • Vancouver, British Columbia, Canada, V5Z 1M9
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    • Manitoba
      • Winnipeg, Manitoba, Canada, R3A 1R9
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    • Ontario
      • Thunder Bay, Ontario, Canada, P7B 6V4
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      • Toronto, Ontario, Canada, M4N 3M5
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    • Quebec
      • Montreal, Quebec, Canada, H4J 1C5
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      • Sherbrook, Quebec, Canada, J1H 5N4
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      • Helsinki, Finland, 00029
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      • Jyvaskyla, Finland, 40620
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      • Kuopio, Finland, 70211
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      • Lahti, Finland, 15850
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      • Seinajoki, Finland, 60220
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      • Tampere, Finland, 33520
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    • Alabama
      • Birmingham, Alabama, Forente stater, 35294
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    • California
      • Loma Linda, California, Forente stater, 92350
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      • Long Beach, California, Forente stater, 90806
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      • San Diego, California, Forente stater, 92123
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    • Colorado
      • Colorado Springs, Colorado, Forente stater, 80920
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      • Denver, Colorado, Forente stater, 80204
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    • Idaho
      • Idaho Falls, Idaho, Forente stater, 83404
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    • Illinois
      • Chicago, Illinois, Forente stater, 60611
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    • Iowa
      • Iowa City, Iowa, Forente stater, 52242
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    • Kansas
      • Topeka, Kansas, Forente stater, 66604
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    • Kentucky
      • Hazard, Kentucky, Forente stater, 41701
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    • Michigan
      • Lansing, Michigan, Forente stater, 48912
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    • Missouri
      • Chesterfield, Missouri, Forente stater, 63017
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      • St Louis, Missouri, Forente stater, 63131
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    • Montana
      • Missoula, Montana, Forente stater, 59802
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    • New York
      • Brooklyn, New York, Forente stater, 11215
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      • Staten Island, New York, Forente stater, 10305
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    • North Carolina
      • Greensboro, North Carolina, Forente stater, 27403
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    • Oregon
      • Portland, Oregon, Forente stater, 97239
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    • Pennsylvania
      • Philadelphia, Pennsylvania, Forente stater, 19107
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      • Pittsburgh, Pennsylvania, Forente stater, 15240
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    • Texas
      • San Antonio, Texas, Forente stater, 78229
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    • Virginia
      • Norfolk, Virginia, Forente stater, 23507
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      • Angers, Frankrike, 49933
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      • Argenteuil, Frankrike, 95107
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      • Bobigny, Frankrike, 93009
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      • Bordeaux, Frankrike, 33076
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      • Dijon, Frankrike, 21079
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      • La Roche Sur Yon, Frankrike, 85000
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      • Le Kremlin Bicetre, Frankrike, 94275
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      • Limoges, Frankrike, 87042
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      • Lyon, Frankrike, 69437
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      • Montpellier, Frankrike, 34295
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      • Nantes, Frankrike, 44093
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      • Nice, Frankrike, 06202
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      • Nimes, Frankrike, 30029
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      • Paris, Frankrike, 75010
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      • Poissy, Frankrike, 78300
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      • Poitiers, Frankrike, 86021
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      • Pringy, Frankrike, 74370
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      • Rennes, Frankrike, 35033
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      • Saint Michel, Frankrike, 16 470
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      • Saint-Etienne, Frankrike, 42055
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      • Toulon, Frankrike, 83056
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      • Tours, Frankrike, 37044
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      • Vandoeuvre-Les-Nancy, Frankrike, 54500
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      • Bangalore, India, 560 002
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      • New Delhi, India, 110 025
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      • Pune, India, 411004
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      • Catania, Italia, 95124
        • 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.
      • Firenze, Italia, 50143
        • 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.
      • Milano, Italia, 20132
        • 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.
      • Monza, Italia, 20052
        • 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.
      • Novara, Italia, 28100
        • 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.
      • Padova, Italia, 35127
        • 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.
      • Rome, Italia, 00168
        • 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.
      • Torino, Italia, 10126
        • 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.
      • Varese, Italia, 21100
        • 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.
      • Mexico City, Mexico, 07760
        • 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.
      • Tlalpan, Mexico, 14000
        • 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.
      • Arnhem, Nederland, 6815 AD
        • 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.
      • Ede, Nederland, 6716 RP
        • 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.
      • Nijmegen, Nederland, 8525 GA
        • 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.
      • Auckland, New Zealand, 1640
        • 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.
      • Christchurch, New Zealand, 8011
        • 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.
      • Grafton, New Zealand, 1023
        • 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.
      • Hamilton, New Zealand, 3204
        • 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.
      • Wellington, New Zealand, 6022
        • 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.
      • Lisbon, Portugal, 1449-005
        • 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.
      • Porto, Portugal, 4202-451
        • 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.
      • Alcala De Henares, Spania, 28805
        • 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.
      • Barcelona, Spania, 08035
        • 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.
      • Burgos, Spania, 9005
        • 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.
      • Getafe, Spania, 28905
        • 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.
      • Las Palmas, Spania, 35010
        • 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.
      • Madrid, Spania, 28040
        • 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.
      • Murcia, Spania, 30008
        • 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.
      • Palma De Mallorca, Spania, 7010
        • 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.
      • Sabadell, Spania, 8208
        • 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.
      • Sevilla, Spania, 41007
        • 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.
      • Tortosa, Spania, 43500
        • 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.
      • Valladolid, Spania, 47012
        • 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.
      • London, Storbritannia, SW17 0QY
        • 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.
    • Avon
      • Bristol, Avon, Storbritannia, BS2 8HW
        • 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.
    • Devon
      • Plymouth, Devon, Storbritannia, PL6 8DH
        • 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.
    • Essex
      • Chelmsford, Essex, Storbritannia, CM2 5ET
        • 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.
    • Hampshire
      • Portsmouth, Hampshire, Storbritannia, P06 3LY
        • 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.
    • Hants
      • Southampton, Hants, Storbritannia, SO16 6YD
        • 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.
    • Scotland
      • Edinburgh, Scotland, Storbritannia, EH4 2XU
        • 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.
      • Glasgow, Scotland, Storbritannia, G42 9TY
        • 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.
    • Surrey
      • Guildford, Surrey, Storbritannia, GU2 7XX
        • 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.
    • West Midlands
      • Birmingham, West Midlands, Storbritannia, B15 2TH
        • 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.
    • West Sussex
      • Chichester, West Sussex, Storbritannia, PO19 6SE
        • 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.
      • Lugano, Sveits, CH-69100
        • 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.
      • St Gallen, Sveits, CH-9007
        • 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.
      • Zurich, Sveits, CH-8091
        • 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.
      • Brno, Tsjekkisk Republikk, 656 91
        • 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.
      • Hradec Kralove, Tsjekkisk Republikk, 500 05
        • 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.
      • Olomouc, Tsjekkisk Republikk, 775 20
        • 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.
      • Plzen, Tsjekkisk Republikk, 304 60
        • 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.
      • Prague, Tsjekkisk Republikk, 128 08
        • 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.
      • Usti Nad Labem, Tsjekkisk Republikk, 40113
        • 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.
      • Aachen, Tyskland, 52074
        • 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.
      • Augsburg, Tyskland, 86156
        • 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.
      • Berlin, Tyskland, 13125
        • 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.
      • Gottingen, Tyskland, 37075
        • 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.
      • Hamburg, Tyskland, 20246
        • 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.
      • Heidelberg, Tyskland, 69120
        • 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.
      • Kiel, Tyskland, 24105
        • 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.
      • Munich, Tyskland, 81377
        • 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.

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inklusjonskriterier:

  • Må være 18 år eller eldre
  • Må ha bevis på infeksjon
  • Må ha systemisk inflammatorisk respons syndrom (SIRS)
  • Må ha vasopressoravhengig septisk sjokk

Ekskluderingskriterier:

  • Har mottatt vasopressorbehandling (i alle doser) i mer enn 24 timer før starten av studiemedikamentet
  • Har sepsis-indusert organdysfunksjon i mer enn 36 timer før starten av studiemedikamentinfusjonen
  • Har enkeltorgandysfunksjon og nylig kirurgi (innen 30 dager etter studiestart)
  • Har hatt kirurgi utført i løpet av 12-timersperioden umiddelbart før studiemedikamentinfusjonen, eller er postoperativ med tegn på aktiv blødning, eller har planlagt eller forventet kirurgi i infusjonsperioden
  • Forventes ikke å overleve 28 dager gitt deres eksisterende ukorrigerbare medisinske tilstand

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: Placebo
0,9 % natriumklorid, intravenøst, 96 timer
Eksperimentell: Drotrecogin alfa (aktivert)
24 mikrogram/kilogram/time, intravenøst, 96 timer (t)
Andre navn:
  • LY203638
  • Xigris

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
28-dagers dødelighet av alle årsaker
Tidsramme: Dag 28
Uttrykt som prosentandel av deltakerne som døde av en hvilken som helst årsak ved endepunktet på dag 28.
Dag 28

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
28-dagers dødelighet av alle årsaker hos deltakere med alvorlig protein C-mangel
Tidsramme: Dag 28
Uttrykt som prosentandel av deltakerne som døde av en hvilken som helst årsak ved endepunktet på dag 28. Deltakere med alvorlig protein C-mangel er de som hadde et protein C-nivå ≤ halvparten av nedre normalgrense (LLN) (≤40 %).
Dag 28
Gjennomsnittlig kardiovaskulær sekvensiell organsviktvurdering (SOFA)-score dag 1 til og med dag 28
Tidsramme: Dag 1 til og med dag 28
Poeng varierer fra 0 (normal) til 4 (organsvikt) med en økende poengsum som indikerer økende kardiovaskulær dysfunksjon. En ikke-overlevende deltaker får en poengsum på 4 (dårligste poengsum) for dødsdagen og hver dag deretter.
Dag 1 til og med dag 28
Gjennomsnittlig vurdering av respiratorisk sekvensiell organsvikt (SOFA) poengsum dag 1 til og med dag 28
Tidsramme: Dag 1 til og med dag 28
Poeng varierer fra 0 (normal) til 4 (organsvikt) med en økende poengsum som indikerer økende respirasjonsdysfunksjon. En ikke-overlevende deltaker får en poengsum på 4 (dårligste poengsum) for dødsdagen og hver dag deretter.
Dag 1 til og med dag 28
Gjennomsnittlig nyresekvensiell organsviktvurdering (SOFA) poengsum dag 1 til og med dag 28
Tidsramme: Dag 1 til og med dag 28
Poeng varierer fra 0 (normal) til 4 (organsvikt) med en økende poengsum som indikerer økende nyredysfunksjon. En ikke-overlevende deltaker får en poengsum på 4 (dårligste poengsum) for dødsdagen og hver dag deretter.
Dag 1 til og med dag 28
90-dagers dødelighet
Tidsramme: Dag 90
Uttrykt som prosentandel av deltakerne som døde av en hvilken som helst årsak ved endepunkt for dag 90.
Dag 90
180-dagers dødelighet
Tidsramme: Dag 180
Uttrykt som prosentandel av deltakerne som døde av en hvilken som helst årsak ved endepunkt for dag 180.
Dag 180
Median overlevelsestid
Tidsramme: Dag 180
Dag 180
EuroQoL Questionnaire-5 Dimensions (EQ-5D) Visual Analog Scale (VAS) score ved baseline, dag 28, 90 og 180
Tidsramme: Baseline og dag 28 og 90 og 180
EQ-5D VAS vurderer omsorgspersonens inntrykk av deltakerens generelle helsetilstand. Poeng varierer fra 0 (dårligste helsetilstand) til 100 (beste helsetilstand), med høyere poengsum som indikerer en bedre helsetilstand.
Baseline og dag 28 og 90 og 180
EuroQoL Questionnaire-5 Dimensions (EQ-5D) Totalpoeng ved baseline, dag 28, 90 og 180
Tidsramme: Baseline og dag 28 og 90 og 180
EQ-5D brukes til å vurdere deltakerens generelle helse. Består av 5 elementer: mobilitet, egenomsorg, vanlige aktiviteter, smerte/ubehag og angst/depresjon. Hvert element har 3 alvorlighetsnivåer (nei, noen, alvorlige problemer). Beregnet fra EQ-5D varierer totalskåren (USA [US] Index Score) fra 0 (dårlig livskvalitet) til 1,00 (beste livskvalitet).
Baseline og dag 28 og 90 og 180
Livskvalitet Short Form-12 (SF-12)-poeng ved baseline, dag 28, 90 og 180
Tidsramme: Baseline og dag 28 og 90 og 180
SF-12 ble brukt som et instrument for å måle deltakernes fysiske velvære (fysisk komponent) og mental velvære (mental komponent). Poeng for hver komponent varierer fra 0-100, med 0 = lavest velvære og 100 = høyest velvære.
Baseline og dag 28 og 90 og 180
Prosentandel av deltakere avbrutt på grunn av uønskede hendelser når som helst fra baseline til dag 28 endepunkt
Tidsramme: Grunnlinje til og med dag 28
Grunnlinje til og med dag 28

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Prosentandel av deltakere med alvorlige blødningshendelser innenfor systemorganklassen når som helst fra baseline til dag 28
Tidsramme: Grunnlinje til og med dag 28
Prosentandelen av deltakerne som opplevde alvorlige blødningshendelser er rapportert etter System Organ Class (SOC) term basert på MedDRA 14.0. For at en blødning skal kvalifisere som en alvorlig hendelse, må den oppfylle standarddefinisjonen av en alvorlig bivirkning eller være en blødning fra sentralnervesystemet eller en blødningshendelse som fører til administrering av ≥3 enheter pakket røde blodlegemer/dag i 2 påfølgende dager.
Grunnlinje til og med dag 28

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. mars 2008

Primær fullføring (Faktiske)

1. september 2011

Studiet fullført (Faktiske)

1. februar 2012

Datoer for studieregistrering

Først innsendt

24. januar 2008

Først innsendt som oppfylte QC-kriteriene

24. januar 2008

Først lagt ut (Anslag)

30. januar 2008

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

18. september 2012

Siste oppdatering sendt inn som oppfylte QC-kriteriene

20. august 2012

Sist bekreftet

1. august 2012

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Andre studie-ID-numre

  • 11940
  • F1K-MC-EVDP (Annen identifikator: Eli Lilly and Company)

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Sepsis

Kliniske studier på Drotrecogin alfa (aktivert)

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