Clinical trial Recruiting at 1 site Interventional Ages 18 and up

OverStitch NXT Endoscopic Suture System for Endoscopic Sleeve Gastrectomy in Obesity

Official title: Gathering of Results in Eligible Asian Obese Populations About Safety and Effectiveness of Overstitch ESG Trial

Run by Boston Scientific Corporation · NCT07276815 · Data updated 2026-11-12

This trial tests whether the OverStitch NXT endoscopic suture system, used with lifestyle management, helps people with obesity lose weight compared to lifestyle management alone.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment136 (estimated)
SponsorBoston Scientific Corporation
Industry-sponsored
Locations1 site (Beijing, China/Beijing)
StatusRecruiting
StartedAugust 6, 2026
Main results expectedOctober 31, 2028
Study endsOctober 31, 2029
Registry record updatedOctober 27, 2026
Trial IDNCT07276815 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older with BMI ≥32.5 kg/m² (or BMI ≥27.5 with type 2 diabetes or with other obesity-related diseases where weight loss is challenging) who are willing to adhere to long-term dietary restrictions and follow-up.

Probably not a fit

Individuals not experiencing weight loss or who are non-responsive to ESG plus lifestyle management may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, multicenter study randomizes adults with obesity to receive ESG using the OverStitch NXT device plus lifestyle management versus lifestyle management alone. A roll-in phase at 10 sites precedes randomization, after which 136 total participants are assigned to treatment or control in a central randomization process. Both groups receive 12 months of follow-up with dietary counseling, and eligible control participants may later undergo ESG. The primary aim is to demonstrate safety and efficacy to support regulatory indication for ESG with OverStitch NXT. The trial is conducted at Beijing Friendship Hospital in China under collaboration with Boston Scientific as sponsor.

Why it matters

Potential benefit: If successful, patients may achieve meaningful weight loss and improved obesity-related health outcomes with ESG using OverStitch NXT.

How similar studies have gone: Prior endoscopic weight-loss approaches have shown promise, but this trial evaluates a specific endoscopic suture system in a randomized design for regulatory indication.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Aged 18 years or older, or subjects who have reached the legal age for signing informed consent in accordance with local laws and regulations.
2. BMI ≥ 32.5 kg/m²; or BMI ≥ 27.5 kg/m² combined with type 2 diabetes mellitus (regardless of the effectiveness of medical treatment for type 2 diabetes); or BMI between 27.5 kg/m² and 32.5 kg/m² with ineffective medical weight loss or combined with other obesity-related diseases for which medical treatment is ineffective.
3. Willing to comply with the long-term strict dietary restrictions required by the surgery.
4. Capable of providing informed consent, able to complete all routine follow-up visits, and willing to abide by the protocol requirements, including signing the informed consent form, completing relevant examinations, and receiving dietary counseling.
5. Females of childbearing potential (i.e., premenopausal or not sterilized) must agree to use adequate contraceptive measures.

Exclusion Criteria:

1. History of foregut or gastrointestinal (GI) surgery (except uncomplicated cholecystectomy or appendectomy)
2. Prior gastrointestinal surgery with sequelae, i.e. obstruction, and/or adhesive peritonitis or known abdominal adhesions.
3. Prior open or laparoscopic bariatric surgery.
4. Prior surgery of any kind on the esophagus or any type of hiatal hernia surgery.
5. Any inflammatory disease of the gastrointestinal tract including severe (LA Grade C or D) esophagitis, gastric ulceration, duodenal ulceration, specific inflammation such as Crohn's disease, and the doctor judges that it may affect the operation or efficacy of ESG.
6. Potential upper gastrointestinal bleeding conditions such as esophageal or gastric varices, congenital or acquired intestinal telangiectasis, or other congenital anomalies of the gastrointestinal tract such as atresia or stenosis.
7. History of gastrointestinal stromal tumors, gastrointestinal cancer, low-grade or high-grade gastric intraepithelial neoplasia, or familial or non-familial adenomatous polyposis syndrome.
8. Gastric masses or untreated gastric polyps with a diameter \> 1 cm.
9. Hiatal hernia (Z-line displacement above the diaphragm \> 4 cm) or severe/refractory gastroesophageal reflux symptoms, which the physician judges may affect the performance or prognosis of ESG.
10. Structural abnormalities of the esophagus or pharynx that may impede endoscopic passage (e.g., strictures or diverticula), which the physician judges may affect the performance or prognosis of ESG.
11. Gastrointestinal motility disorders (e.g., achalasia, severe esophageal motility disorders, gastroparesis, or intractable constipation), which the physician judges may affect the performance or prognosis of ESG.
12. Evidence of untreated psychiatric or eating disorders, such as major depression, schizophrenia, substance abuse, binge eating disorder, or bulimia nervosa.
13. Coagulopathy with INR \> 1.5 that cannot be corrected (per physician's judgment) or requirement for continuous full anticoagulant therapy, and/or any underlying diseases associated with high bleeding risk.
14. Insulin-dependent diabetes mellitus (type 1 or type 2), or high likelihood of requiring insulin therapy within the next 12 months.
15. Decompensated cirrhosis, or acute/chronic liver dysfunction that the physician judges make the subject unsuitable for ESG treatment.
16. Diagnosis of autoimmune connective tissue diseases (e.g., systemic lupus erythematosus, scleroderma) or immunocompromise, which the physician assesses may affect the performance or prognosis of ESG.
17. Known history of endocrine diseases affecting body weight (e.g., Cushing's syndrome, uncontrolled hypothyroidism, or hyperthyroidism), which the physician assesses may affect the performance or prognosis of ESG.
18. Anemia: Hemoglobin (Hgb) \< 110 g/L for females; Hgb \< 120 g/L for males.
19. Any other medical conditions precluding elective endoscopy, such as poor general health, history of severe renal, hepatic, cardiac, and/or pulmonary diseases, and/or severe or uncontrolled psychiatric illnesses or abnormalities that may impair the patient's ability to understand or comply with follow-up visits and lifestyle interventions.
20. Active psychological issues as determined by a psychologist or psychiatrist, precluding participation in lifestyle modification programs.
21. Unwillingness to participate in the established medically supervised dietary and behavioral modification programs, as well as routine medical follow-up.
22. Daily treatment with prescribed high-dose aspirin (\> 80 mg per day), non-steroidal anti-inflammatory drugs (NSAIDs), antiplatelet agents, anticoagulants, corticosteroids, immunosuppressants, or other gastric irritant medications.
23. Interval use of medications that may be affected by changes in gastric emptying (e.g., antiepileptic drugs or antiarrhythmic drugs).
24. Inability or unwillingness to take prescribed proton pump inhibitor (PPI) medications.
25. Current use of weight loss medications or other weight loss devices or use within the past 90 days.
26. Current participation in a clinical trial involving investigational drugs or devices, or participation in such a trial within 30 days prior to enrollment in this study.
27. Use of intragastric devices within 30 days prior to this study, which the physician assesses may affect the performance or prognosis of ESG.
28. Unwillingness to avoid any reconstructive and/or plastic surgeries that may affect body weight during the study (e.g., mammoplasty, liposuction).
29. Other conditions deemed unsuitable for endoscopy or ESG treatment by the investigator, including but not limited to conditions that the investigator believes may expose the subject to significant risks, confound study results, increase risks associated with endoscopy and/or endoscopic procedures, or substantially interfere with the subject's participation in the study.
30. Pregnancy, lactation, or intention to become pregnant during the study (for females of childbearing potential).

Where it's running

  • Beijing Friendship Hospital, Affiliated to Capital Medical University
    Beijing, China/Beijing, China
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.