Individualized Obesity Pharmacotherapy
Part of paid clinical trials in Rochester, Minnesota.
- Sponsor
- Mayo Clinic
- Study ID
- NCT03374956
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Phentermine-Topiramate — DRUGExtended Release at dose of 7.5/46 mg oral daily
- Liraglutide — DRUGdose of 3 mg subcutaneous daily
- Naltrexone/bupropion — DRUGOral naltrexone extended-release/bupropion extended-release at dose of 32/360 mg oral daily (divided in 2 tables in morning and 2 tablets in evening)
- Phentermine — DRUG15-37.5 mg oral daily
Study Details
The researchers are trying to identify the specific characteristics (phenotypes) that may be useful to help select the right medication for weight loss.
Key Dates
- Start date
- Dec 11, 2017
- Status verified
- Jun 2023
- Primary completion
- May 26, 2022
- Completion
- May 26, 2022
Study Design
- Enrollment
- 193 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Intervention groupPhenotype-guided pharmacotherapy, which includes Phentermine-Topiramate, Liraglutide, Naltrexone/bupropion or Phentermine plus Exercise
- Active Comparator: Control GroupRandomly assigned pharmacotherapy, which includes Phentermine-Topiramate, Liraglutide, Naltrexone/bupropion or Phentermine
Primary Outcome Measure
Change in Total Body Weight [ Time Frame: baseline to 12 weeks ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Mayo Clinic in Rochester | Rochester | Minnesota | 55905 | - |
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