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New No-Cut weight loss procedure tested in chinese adults

NCT ID NCT07237750

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a new, non-surgical procedure called Endoscopic Radial Compression Gastroplasty (ERCG) that uses a clip-and-loop system to reduce stomach size, helping with weight loss. It is for Chinese adults aged 18-65 with a BMI of 24.0-37.4 who have not succeeded with diet and exercise alone. Participants will either receive the ERCG procedure plus lifestyle coaching or a sham procedure plus lifestyle coaching, and weight loss will be tracked for 6 months.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 216 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2026

Expected to finish

May 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Asian adults aged 18-65 years. * BMI 24.0-37.4kg/m²(Chinese standard)。 * Failed prior conservative weight loss attempts ≥2 months。 * Willingness to comply with follow-up. * Provided written informed consent. Exclusion Criteria: * Prior gastrointestinal surgery with clinically relevant sequelae. * 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. * Esophageal/pharyngeal structural abnormalities that may impede endoscope passage (e.g., stricture, diverticulum). * Achalasia or other severe esophageal motility disorder. * Severe coagulopathy. * Insulin-dependent diabetes mellitus. * Chronic abdominal pain. * Gastrointestinal motility disorder (e.g., gastroparesis). * Hepatic impairment or cirrhosis. * Severe or uncontrolled psychiatric illness. * 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. * 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. * Known or suspected hypersensitivity to any material/component of the study system. * Pregnant or breastfeeding. * Severe cardiopulmonary disease or other serious systemic/organic disease. * Positive Helicobacter pylori (H. pylori) test. * 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. * Participation in a weight-affecting clinical trial within the past 6 months. * 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).

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • The fifth Medical Center of Chinese PLA General Hospital, Beijing

    NOT_YET_RECRUITING

    Beijing, Beijing Municipality, 100073, China

  • The fifth Medical Center of Chinese PLA General Hospital, Beijing

    RECRUITING

    Beijing, Beijing Municipality, 100073, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.