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NCT07336862RecruitingPhase 1/2

Bariatric Surgery Combined With GLP-1 Receptor Agonists Study

The Efficacy and Safety of Bariatric Surgery Combined With GLP-1 Receptor Agonists for Patients With Severe Obesity: A Prospective, Multicenter Cohort Study

Source: ClinicalTrials.gov · Last updated 23 Apr 2026

Brief summary (registry, in English)

Obese patients exhibit considerable heterogeneity and complex comorbidities, making long-term effective management challenging with single therapies. While bariatric surgery remains the most effective weight-loss intervention, postoperative weight regain and metabolic deterioration require attention. GLP-1 RAs offer distinct advantages for weight and metabolic improvement, and their combined application with surgery may yield synergistic benefits. This study investigates the efficacy and safety of bariatric surgery combined with GLP-1 receptor agonist adjuvant therapy for severe obesity.

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
200 (estimated)
First submitted
29 Sept 2025
Start date
1 Jan 2024
Primary completion date
Dec 2027
Lead sponsor
China-Japan Friendship Hospital
Diseases
Obesity
NCT number
NCT07336862

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 200
  • From 1 Jan 2024 to the primary completion date, Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Recent GLP-1RA use: Treatment with GLP-1 receptor agonists within 6 months preoperatively
  • Prior bariatric surgery: History of any metabolic/bariatric surgical procedure
  • Non-indicated candidates: Patients not meeting standard bariatric surgery indications

Other illness

  • Postoperative complications: Requiring reoperation for severe complications (e.g., hemorrhage, anastomotic leak)

Lab values

  • Significant comorbidities:
    • Advanced hepatic/renal dysfunction (Child-Pugh C or eGFR \<30 mL/min/1.73m²)
    • Active malignancy (except non-melanoma skin cancers)
    • Autoimmune disorders requiring immunosuppression
    • Uncontrolled psychiatric conditions (e.g., active psychosis, severe depression)

Who the study is looking for

  • Primary metabolic surgery candidates: Patients undergoing initial laparoscopic sleeve gastrectomy (LSG)
  • obesity:BMI ≥35 kg/m²
  • Metabolic comorbidities: Diagnosis of metabolic syndrome or type 2 diabetes mellitus (T2DM) meeting standard criteria
  • Age range: 18-60 years (inclusive)
  • Informed consent: Willing participation with documented consent

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
China-Japan Friendship Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.