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liraglutide glp 1 agonist cohort n=100 2023-09-01 ClinicalTrials

Observational Study Investigates Optimal Liraglutide Timing for Post-Bariatric Surgery Obesity Management

Research on Timing of Liraglutide Therapy in Patients With Obesity After Metabolic Surgery

Background

Obesity remains a significant global health challenge, often requiring interventions like metabolic surgery for sustained weight loss and remission of comorbidities. While highly effective, a notable subset of patients experiences insufficient initial weight loss or subsequent weight regain, leading to persistent obesity. This can compromise the long-term benefits of surgery and necessitate further interventions. Current post-surgical management primarily focuses on lifestyle modifications, but pharmacological adjuncts are gaining importance. Glucagon-like peptide-1 (GLP-1) receptor agonists, such as liraglutide, have demonstrated robust efficacy in promoting weight loss and improving metabolic health by enhancing satiety, slowing gastric emptying, and reducing food intake. However, the optimal timing and integration of these powerful agents into the post-bariatric surgery care pathway, particularly for patients with suboptimal weight outcomes, remain an area of active investigation and clinical uncertainty. This observational study directly addresses this critical clinical gap.

Study Design

Population
100 patients who remained obese six months after metabolic surgery.
Intervention
Liraglutide, initiated at 0.6 mg/day and titrated weekly by 0.6 mg up to a maximum tolerated dose of 3.0 mg/day once daily for 24 weeks.
Comparator
Control group receiving only diet and exercise guidance.
Outcome
Optimal liraglutide timing for post-bariatric surgery obesity management.

This observational study enrolled 100 patients who remained obese six months after metabolic surgery. Participants were assigned to one of three arms: a control group receiving only diet and exercise guidance, a group initiating liraglutide at enrollment for 6 months, and a third group (partially described as "Lir"). The liraglutide regimen started at 0.6 mg/day and was titrated weekly by 0.6 mg up to a maximum tolerated dose of 3.0 mg/day once daily for 24 weeks. All groups received diet and exercise guidelines. The study is non-randomized and observational, focusing on real-world outcomes.


liraglutide glp 1 agonist glp-1r dose mentioned protocol relevant
Source: clinicaltrials:NCT07374445 · Ingested 2026-05-21 · Digest: gemini-2.5-flash