Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 60Years
All Genders
NCT07336862

Bariatric Surgery Combined With GLP-1 Receptor Agonists Study

Led by China-Japan Friendship Hospital · Updated on 2026-04-23

200

Participants Needed

1

Research Sites

204 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Bariatric Surgery Combined With GLP-1 Receptor Agonists Study

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing their first laparoscopic sleeve gastrectomy (primary metabolic surgery candidates)
  • Body mass index (BMI) of 35 kg/m² or greater
  • Diagnosis of metabolic syndrome or type 2 diabetes mellitus according to standard criteria
  • Age between 18 and 60 years inclusive
  • Willing to participate and provide documented informed consent
Not Eligible

You will not qualify if you...

  • Treatment with GLP-1 receptor agonists within 6 months before surgery
  • History of any metabolic or bariatric surgery
  • Postoperative complications requiring reoperation, such as hemorrhage or anastomotic leak
  • Not meeting standard indications for bariatric surgery
  • Advanced liver or kidney problems (Child-Pugh C liver disease or kidney function below eGFR 30 mL/min/1.73m²)
  • Active cancer except for non-melanoma skin cancers
  • Autoimmune diseases needing immunosuppressive treatment
  • Uncontrolled psychiatric conditions like active psychosis or severe depression

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

China-Japan Friendship Hospital

Beijing, China

Actively Recruiting

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Research Team

Y

Yishan Huang, Ph.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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