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NCT07237750Recruiting

iWAIST Trial: ERCG (Endoscopic Radial Compression Gastroplasty) +Optimized Lifestyle Intervention (OLI) vs Sham + OLI for Weight Loss

iWAIST Trial: A Multicenter, Single-Blind, Randomized, Sham-Controlled Trial of Endoscopic Radial Compression Gastroplasty (ERCG) Plus Optimized Lifestyle Intervention for Weight Management in Chinese Adults With Overweight or Mild-to-Moderate Obesity

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

This randomized, sham-controlled trial evaluates the efficacy and safety of ERCG plus optimized lifestyle intervention compared with sham procedure plus optimized lifestyle intervention in Chinese adults with overweight accompanied by at least one metabolic comorbidity or with mild-to-moderate obesity. The co-primary outcomes are percentage total weight loss (%TWL) at 12 weeks and the clinical response rate at 12 weeks, defined as the proportion of participants achieving %TWL ≥5%. Secondary outcomes include weight-related, metabolic, hepatic steatosis-related, imaging, symptom, quality-of-life, and safety outcomes.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
216 (estimated)
First submitted
16 Sept 2025
Start date
13 Mar 2026
Primary completion date
30 Mar 2027
Lead sponsor
Liu Yan
NCT number
NCT07237750

What you commit to

  • Study type: Interventional
  • Planned participants: 216
  • From 13 Mar 2026 to the primary completion date, 30 Mar 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, not your situation.

Who cannot take part

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

Prior treatment

  • Prior gastrointestinal surgery with clinically relevant sequelae.
  • Daily regular use of NSAIDs, anticoagulants, or other gastric-irritating medications.
  • Unable or unwilling to take proton pump inhibitor (PPI) therapy as prescribed during the treatment period.
  • Use of time-critical medications potentially affected by altered gastric emptying (e.g., antiepileptics, antiarrhythmics).
  • Current systemic corticosteroids, immunosuppressants, or opioid analgesics.
  • Use of any weight-loss medication within the past 3 months or current use.
  • Prior use of any intragastric device.

Other illness

  • Active or clinically significant gastrointestinal disease, including inflammatory conditions (e.g., esophagitis, Barrett's esophagus, Crohn's disease), peptic ulcer disease (gastric/duodenal ulcer), or neoplastic lesions.
  • Any condition associated with an increased risk of upper gastrointestinal bleeding.
  • Hiatal hernia \>2 cm or severe/refractory gastroesophageal reflux disease (GERD); acid reflux requiring ≥2 medications for symptom control.
  • Achalasia or other severe esophageal motility disorder.
  • Insulin-dependent diabetes mellitus.
  • Gastrointestinal motility disorder (e.g., gastroparesis).
  • Hepatic impairment or cirrhosis.
  • Severe or uncontrolled psychiatric illness.
  • Known or suspected hypersensitivity to any material/component of the study system.
  • Severe cardiopulmonary disease or other serious systemic/organic disease.
  • Active infection not successfully eradicated before enrolment.
  • Symptomatic congestive heart failure, clinically significant arrhythmia, or unstable coronary artery disease.
  • Clinically significant respiratory disease.
  • Autoimmune connective tissue disease.
  • Life expectancy \<1 year or severe renal/hepatic/pulmonary or other serious medical illness.
  • Known genetic or endocrine cause of obesity (e.g., hypothyroidism, Prader-Willi syndrome) or other endocrine disease known to affect body weight.
  • Eating disorder (e.g., night eating syndrome, bulimia nervosa, binge eating disorder, compulsive eating).

Other

  • Esophageal/pharyngeal structural abnormalities that may impede endoscope passage (e.g., stricture, diverticulum).
  • Severe coagulopathy.
  • Chronic abdominal pain.
  • Alcohol abuse or substance dependence.
  • Unwilling to participate in a physician-supervised diet/behavior modification program and/or unwilling to comply with routine follow-up.
  • Pregnant or breastfeeding.
  • Participation in a weight-affecting clinical trial within the past 6 months.

Who the study is looking for

  • Asian adults aged 18-65 years.
  • BMI 24.0-27.9 with ≥ 1 obesity-related complication
  • BMI 28.0-37.4kg/m²
  • Failed prior conservative weight loss attempts
  • Willingness to comply with follow-up.
  • Provided written informed consent.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The fifth Medical Center of Chinese PLA General Hospital, Beijing
Coordinator of this site? Confirm its status
BeijingChinaNot yet recruiting

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