Evaluation of Liraglutide 3.0mg in Patients With Poor Weight-loss and a Suboptimal Glucagon-like Peptide-1 Response
NCT03341429 · Completed
Last updated 2026-05-28This clinical trial tested the medication liraglutide at a 3.0mg dose in adults with obesity who had poor weight loss and a weak response to a natural gut hormone called GLP-1.
Status Completed The study has finished.
Phase Phase 4 Monitors a drug already on the market.
Type Interventional (clinical trial)
Design Randomized, quadruple-blind treatment study
Participants 70 people
Who can join Ages 18–64 · all sexes
Timeline Started 2018-08 · est. completion 2020-06
Where 1 site · United Kingdom
What this study is testing ClinicalTrials.gov NCT03341429 ↗
Description as written by the study sponsor.
A double-blinded, randomised, placebo-controlled trial of liraglutide 3.0 mg in patients with poor weight-loss and a suboptimal glucagon-like peptide-1 response following bariatric surgery
Treatments tested
- Liraglutide Pen Injector [Saxenda] also known as Saxenda Drug
Daily injection of GLP-1 agonist (liraglutide 3.0 mg) for obese patients presenting poor weight loss (\<20%) after bariatric surgery and suboptimal GLP-1 levels.
- Placebo Drug
Daily subcutaneous injection
| Main thing measured | %WL |
|---|---|
| Sponsor | University College, London |
| Conditions studied | Obesity |
| GLP-1 drugs | liraglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT03341429 ↗