- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01660035
The Product Surveillance Registry REVERSE Post Approval Study (PSR-REVERSE)
15. april 2022 opdateret af: Medtronic
The REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction (REVERSE) Post Approval Study
The purpose of the REVERSE Post Approval Study (PAS) is to confirm the benefit observed in the REVERSE and RAFT pivotal studies in "real-world" clinical practice.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
The REVERSE PAS will estimate the 3-year survival probability of freedom from heart failure hospitalization and heart failure events in patients implanted with a Medtronic CRT-D device who meet the expanded indication criteria with a QRS duration ≤ 150 ms.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
155
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Leuven, Belgien
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Alberta
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Calgary, Alberta, Canada, T2N 4N1
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Ontario
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London, Ontario, Canada
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Ottawa, Ontario, Canada
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Quebec
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Montreal, Quebec, Canada
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Quebec City, Quebec, Canada
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Liverpool, Det Forenede Kongerige
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Middlesborough, Det Forenede Kongerige
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Alabama
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Birmingham, Alabama, Forenede Stater, 35294
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Alaska
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Anchorage, Alaska, Forenede Stater, 99508
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Arizona
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Chandler, Arizona, Forenede Stater, 85226
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Gilbert, Arizona, Forenede Stater, 85295
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Arkansas
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Jonesboro, Arkansas, Forenede Stater, 72410
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Little Rock, Arkansas, Forenede Stater, 72205
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California
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Bakersfield, California, Forenede Stater, 93301
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Chula Vista, California, Forenede Stater, 91910
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Los Angeles, California, Forenede Stater, 90048
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Rancho Mirage, California, Forenede Stater, 92270
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Redwood City, California, Forenede Stater, 94062
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Salinas, California, Forenede Stater, 93901
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San Diego, California, Forenede Stater, 92103
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Stanford, California, Forenede Stater, 94305
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Torrance, California, Forenede Stater, 90503
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Van Nuys, California, Forenede Stater, 91405
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Colorado
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Colorado Springs, Colorado, Forenede Stater, 80907
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Lakewood, Colorado, Forenede Stater, 80228
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Connecticut
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New Haven, Connecticut, Forenede Stater, 06519
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District of Columbia
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Washington, District of Columbia, Forenede Stater, 20010
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Florida
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Bradenton, Florida, Forenede Stater, 34205
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Clearwater, Florida, Forenede Stater, 33756
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Jacksonville, Florida, Forenede Stater, 32216
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Safety Harbor, Florida, Forenede Stater, 34695
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Georgia
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Albany, Georgia, Forenede Stater, 31701
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Atlanta, Georgia, Forenede Stater, 30308
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Marietta, Georgia, Forenede Stater, 30060
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Indiana
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Evansville, Indiana, Forenede Stater, 47710
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Iowa
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West Des Moines, Iowa, Forenede Stater, 50266
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Kansas
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Kansas City, Kansas, Forenede Stater, 66160
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Kentucky
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Edgewood, Kentucky, Forenede Stater, 41017
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Lexington, Kentucky, Forenede Stater, 40503
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Louisville, Kentucky, Forenede Stater, 40207
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Louisiana
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Baton Rouge, Louisiana, Forenede Stater, 70808
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Maryland
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Hyattsville, Maryland, Forenede Stater, 20782
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Salisbury, Maryland, Forenede Stater, 21804
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Silver Spring, Maryland, Forenede Stater, 20910
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Takoma Park, Maryland, Forenede Stater, 20912
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Michigan
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Lansing, Michigan, Forenede Stater, 48912
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Marquette, Michigan, Forenede Stater, 49855
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Ypsilanti, Michigan, Forenede Stater, 48197
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Minnesota
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Coon Rapids, Minnesota, Forenede Stater, 55433
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Minneapolis, Minnesota, Forenede Stater, 55407
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Robbinsdale, Minnesota, Forenede Stater, 55422
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Rochester, Minnesota, Forenede Stater, 55905
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Saint Cloud, Minnesota, Forenede Stater, 56303
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Saint Paul, Minnesota, Forenede Stater, 55102
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Mississippi
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Hattiesburg, Mississippi, Forenede Stater, 39401
- Hattiesburg Clinic
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Missouri
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Columbia, Missouri, Forenede Stater, 65201
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Kansas City, Missouri, Forenede Stater, 64111
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New Hampshire
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Lebanon, New Hampshire, Forenede Stater, 03766
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New Jersey
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Morristown, New Jersey, Forenede Stater, 07960
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Ocean City, New Jersey, Forenede Stater, 07712
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Ridgewood, New Jersey, Forenede Stater, 07450
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New Mexico
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Albuquerque, New Mexico, Forenede Stater, 87106
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New York
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Bay Shore, New York, Forenede Stater, 11706
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Bronx, New York, Forenede Stater
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Huntington, New York, Forenede Stater, 11743
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Manhasset, New York, Forenede Stater, 11030
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New Hyde Park, New York, Forenede Stater, 11040
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New York, New York, Forenede Stater, 10075
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Poughkeepsie, New York, Forenede Stater, 12601
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Staten Island, New York, Forenede Stater, 10305
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Utica, New York, Forenede Stater, 13501
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North Carolina
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Charlotte, North Carolina, Forenede Stater, 28203
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Durham, North Carolina, Forenede Stater, 27705
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Raleigh, North Carolina, Forenede Stater, 27610
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Ohio
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Akron, Ohio, Forenede Stater, 44304
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Cincinnati, Ohio, Forenede Stater, 45219
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Cleveland, Ohio, Forenede Stater, 44195
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Columbus, Ohio, Forenede Stater, 43210
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Toledo, Ohio, Forenede Stater, 43608
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Oklahoma
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Oklahoma City, Oklahoma, Forenede Stater, 73120
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Oregon
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Portland, Oregon, Forenede Stater, 97220
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Pennsylvania
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Allentown, Pennsylvania, Forenede Stater, 18103
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Bethlehem, Pennsylvania, Forenede Stater, 18017
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Danville, Pennsylvania, Forenede Stater, 17822
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Erie, Pennsylvania, Forenede Stater, 16550
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Lancaster, Pennsylvania, Forenede Stater, 17604
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Philadelphia, Pennsylvania, Forenede Stater, 19104
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Pittsburgh, Pennsylvania, Forenede Stater, 15213
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Wilkes-Barre, Pennsylvania, Forenede Stater, 18711
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Wynnewood, Pennsylvania, Forenede Stater, 19096
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South Carolina
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Columbia, South Carolina, Forenede Stater, 29204
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Tennessee
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Germantown, Tennessee, Forenede Stater, 38138
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Nashville, Tennessee, Forenede Stater, 37212
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Texas
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Austin, Texas, Forenede Stater, 78705
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Dallas, Texas, Forenede Stater, 75226
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Fort Worth, Texas, Forenede Stater, 76104
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Houston, Texas, Forenede Stater, 77030
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Plano, Texas, Forenede Stater, 75093
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San Antonio, Texas, Forenede Stater, 78229
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The Woodlands, Texas, Forenede Stater, 77384
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Vermont
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Burlington, Vermont, Forenede Stater, 05401
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Virginia
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Charlottesville, Virginia, Forenede Stater, 22908
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Falls Church, Virginia, Forenede Stater, 22042
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Leesburg, Virginia, Forenede Stater, 20176
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Washington
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Olympia, Washington, Forenede Stater, 98506
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Spokane, Washington, Forenede Stater, 99204
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Tacoma, Washington, Forenede Stater, 98402
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Wisconsin
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Madison, Wisconsin, Forenede Stater, 53715
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Milwaukee, Wisconsin, Forenede Stater, 53215
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La Rochelle, Frankrig
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Nantes, Frankrig
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Eindhoven, Holland
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Maastricht, Holland
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Nieuwegein, Holland
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Rotterdam, Holland
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Reggio Emilia, Italien
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Zurich, Schweiz
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Skovde, Sverige
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Essen, Tyskland
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Hannover, Tyskland
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Homburg, Tyskland
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Ulm, Tyskland
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Heart failure patients that are implanted with a Medtronic CRT-D device and meet the expanded indication criteria.
Beskrivelse
Inclusion Criteria:
- Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements
- Patient has or is intended to receive or be treated with a Medtronic CRT-D who meets the expanded CRT-D indication criteria with a QRS ≤ 150ms
- Patient within 30 days of implant
Exclusion Criteria:
- Patient who is, or will be, inaccessible for follow-up
- Patient with exclusion criteria required by local law
- Patient is currently enrolled in or plans to enroll in any concurrent drug and/or device study that may confound results
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Survival from Heart Failure Hospitalization and All-Cause Mortality
Tidsramme: 3 years
|
To estimate the 3-year survival probability of freedom from heart failure hospitalization or all-cause death for patients implanted with a Medtronic CRT-D device meeting the approved expanded indication criteria with a QRS duration ≤ 150ms.
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3 years
|
|
Survival from Heart Failure Event and All-Cause Mortality
Tidsramme: 3 years
|
To estimate the 3-year survival probability of freedom from heart failure event or all- cause death for patients implanted with a Medtronic CRT-D device meeting the approved expanded indication criteria with a QRS duration ≤ 150ms.
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3 years
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. april 2012
Primær færdiggørelse (Faktiske)
1. april 2022
Studieafslutning (Faktiske)
1. april 2022
Datoer for studieregistrering
Først indsendt
6. august 2012
Først indsendt, der opfyldte QC-kriterier
6. august 2012
Først opslået (Skøn)
8. august 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
18. april 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
15. april 2022
Sidst verificeret
1. april 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- PSR-REVERSE
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Hjertefejl
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Fondation Hôpital Saint-JosephRekruttering
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Region SkaneTilmelding efter invitationHjertesvigt New York Heart Association (NYHA) klasse II | Hjertesvigt New York Heart Association (NYHA) klasse IIISverige
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Medical University of BialystokMedical University of Lodz; Poznan University of Medical Sciences; Nicolaus... og andre samarbejdspartnereAfsluttetHjertesvigt, systolisk | Hjertesvigt med reduceret udstødningsfraktion | Hjertesvigt New York Heart Association Klasse IV | Hjertesvigt New York Heart Association Klasse IIIPolen
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Portuguese Association of Interventional CardiologyMedtronicRekrutteringSvær Symptomatisk Aortastenose (Defineret som New York Heart Association (NYHA) klasse ≥ II)Portugal
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University of WashingtonAmerican Heart AssociationAfsluttetHjertesvigt, Kongestiv | Mitokondriel ændring | Hjertesvigt New York Heart Association Klasse IVForenede Stater
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Novartis PharmaceuticalsAfsluttetPatienter, der med succes afslutter den 12-måneders behandlingsperiode i kernestudiet (de Novo Heart-modtagere), som var interesserede i at blive behandlet med EC-MPS
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University Hospital, GasthuisbergUkendtTransient Left Ventricular Ballooning SyndromeBelgien
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NYU Langone HealthRekrutteringTako-tsubo kardiomyopati | Takotsubo kardiomyopati | Broken Heart SyndromeForenede Stater
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French Cardiology SocietyAfsluttet