Functional Impact of GLP-1 for Heart Failure Treatment (FIGHT)
Part of paid clinical trials in Newark, Delaware.
- Sponsor
- Duke University
- Study ID
- NCT01800968
- Phase
- PHASE2
- Status
- Completed
Conditions
- Acute Heart Failure
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Liraglutide — DRUGActive Drug
- Placebo — DRUGPlacebo
Study Details
The primary objective is to test the hypothesis that, compared with placebo, therapy with Subcutaneous (SQ) GLP-1 agonist in the post-Acute Heart Failure Syndrome (AHFS) discharge period will be associated with greater clinical stability at six months as assessed by a composite clinical endpoint.
Key Dates
- Start date
- Apr 30, 2013
- Status verified
- Feb 2017
- Primary completion
- Oct 31, 2015
- Completion
- Oct 31, 2015
Study Design
- Enrollment
- 300 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: LiraglutideIncreasing dose from 0.6mg, 1.2mg to 1.8mg SQ daily.
- Placebo Comparator: PlaceboPlacebo dose increasing from 0.6mg, 1.2mg to 1.8 mg SQ daily.
Primary Outcome Measure
Global Ranking of Predefined Events [ Time Frame: Randomization to 180 days ]
Locations (25)
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