Is Saxenda® a Viable Treatment of Obese Patients in Forensic Psychiatry?
NCT04781998 · Completed
Last updated 2026-05-28This clinical trial is testing whether Saxenda® (liraglutide) can be a feasible treatment for weight loss in overweight or obese patients receiving care in forensic psychiatric settings.
What this study is testing ClinicalTrials.gov NCT04781998 ↗
Description as written by the study sponsor.
An open-label, multi-centre, 26-weeks clinical feasibility study. The objective is to explore whether Saxenda could be a feasible choice in the treatment of overweight, obesity and weight-related medical problems, in patients diagnosed with a severe mental illness and hospitalized at a forensic department in Denmark. We wish to determine the viability of the daily Saxenda®-injection treatment in this specific patient group.
Treatments tested
- liraglutide 3 mg (Saxenda®) once-daily Drug
Liraglutide 3 mg (Saxenda®) 6 mg/ml, 3 ml pre-filled pen-injector. The injection is administered subcutaneously. The initial daily dose will be 0.6 mg liraglutide (Saxenda®) for one week. If tolerated patients increase the dose by +0.6 mg each week until the full maintenance of 3 mg is reached (week 1: 0.6 mg, week 2: 1.2 mg, week 3: 1.8 mg, week 4: 2.4 mg, week 5-26: 3.0 mg. If necessary, a longer titration period is accepted). If the lowest tolerated dose is less than 1.8 mg of liraglutide (Saxenda®) once-daily after 12 weeks from inclusion, the patient will be excluded from the study.
| Main thing measured | The primary endpoint is the number of "completers" |
|---|---|
| Sponsor | Anders Fink-Jensen, MD, DMSci |
| Conditions studied | Mental Disorder, Metabolic Disturbance, Feasibility, Overweight and Obesity, Liraglutide |
| GLP-1 drugs | liraglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT04781998 ↗