Saxenda in Obesity Services (STRIVE Study)
NCT03036800 · Completed
Last updated 2026-05-28This clinical trial is testing the effectiveness of the medication Saxenda in helping adults with obesity or diabetes lose at least 15% of their body weight.
What this study is testing ClinicalTrials.gov NCT03036800 ↗
Description as written by the study sponsor.
A two year, parallel, two group, open-label, real-world randomised controlled trial (RCT) design for subjects with severe and complex obesity who are referred to a Tier 3 or equivalent specialist weight management/obesity service. Participants will be randomised to receive 1) standard care (obesity-specialist care), or 2) targeted prescribing pathway (obesity-specialist care plus targeted use of Liraglutide 3.0mg \[LIRA 3mg\] with pre-specified stopping rules for the medication). The aim of the study is to compare the effectiveness, budget impact, and cost-effectiveness between the two groups in a real-world setting among otherwise largely unselected patients.
Treatments tested
- Saxenda also known as Liraglutide 3mg Drug
standard care plus targeted use of Liraglutide (LIRA) 3mg when pre-specified stopping rules for the medication apply. Liraglutide (Saxenda) 6 mg/mL solution for injection in pre-filled pen, administered by subcutaneous injection. Dose escalation to 3.0 mg daily (or maximum tolerated dose)
- Specialist Obesity Management Services Other
Specialist Obesity Management Services standard of care
| Main thing measured | Weight Loss of ≥15% From Baseline (Complete Cases) |
|---|---|
| Sponsor | University of Leicester |
| Conditions studied | Obesity, Weight Loss, Diabetes Mellitus |
| GLP-1 drugs | liraglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT03036800 ↗