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NCT05711758Recruiting

Efficacy and Safety of Endoscopic Antral Myotomy as a Novel Weight Loss Procedure

Efficacy and Safety of Endoscopic Antral Myotomy as a Novel Weight Loss Procedure: A Pilot Study

Source: ClinicalTrials.gov · Last updated 2 Mar 2026

Brief summary (registry, in English)

Gastric myotomy has been performed for several years as a means of addressing chronic stenosis after sleeve gastrectomy and treating gastroparesis. The Pylorus Sparing Antral Myotomy (PSAM) technique has the opposite effect by leaving the pylorus intact and extending the myotomy proximally to the distal gastric body. PSAM was initially combined with ESG and shown to delay gastric emptying and provide greater weight loss without impacting tolerability (GCSI score) or the safety profile of the procedure (2 DDW GEM abstracts). PSAM has not been evaluated alone, without concomitant ESG. Since delayed gastric emptying alone is known to promote weight loss, it is thought that PSAM alone (without ESG) may provide similar efficacy, while reducing procedure time and adverse events. There have been no clinical studies that investigate the efficacy of PSAM independent of ESG. This pilot study aims to address this lack of information by evaluating the safety, tolerability, and short-term efficacy of PSAM, in addition to exploring its impact on gastric physiology. This will also provide data that may be used in designing a larger clinical trial.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
29 Dec 2022
Start date
22 Sept 2023
Primary completion date
Dec 2026
Lead sponsor
Christopher C. Thompson, MD, MSc
Diseases
Obesity
NCT number
NCT05711758

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 22 Sept 2023 to the primary completion date, Dec 2026
  • 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

  • an ongoing or a history of treatment with opioids in the last 12 months prior to enrollment
  • previous pyloromyotomy or pyloroplasty
  • use of any medication that may interfere with weight loss
  • use of any medication that may interfere with gastric emptying

Other illness

  • untreated H. pylori infection
  • any inflammatory disease of the gastrointestinal tract (including but not limited to severe (LA Grade C or D) esophagitis, active gastric ulceration, active duodenal ulceration, or specific inflammation such as Crohn's disease)
  • malignant or premalignant gastric diseases (such as high grade dysplasia, gastric cancer, or GIST)
  • severe cardiopulmonary disease or a history of coronary artery disease (including myocardial infarction within the past 6 months, poorly controlled hypertension, required use of NSAIDs)
  • history of gastrointestinal surgery
  • any serious health condition unrelated to their weight that would increase the risk of endoscopy
  • a known history of endocrine disorders affecting weight (uncontrolled hypothyroidism)
  • any other condition which the investigator may deem as an impediment to compliance or hinder completion of the proposed study

Other

  • gastroparesis
  • active smoking
  • gastrointestinal obstruction
  • severe coagulopathy
  • esophageal or gastric varices and/or portal hypertensive gastropathy
  • pregnancy or puerperium
  • lactation
  • chronic abdominal pain
  • active psychological issues preventing participation in a lifestyle modification program
  • an inability to provide informed consent

Who the study is looking for

  • subjects must be 18-70 years of age
  • eligible for endoscopic and surgical weight loss procedures
  • body mass index (BMI) greater than 35 kg/m2
  • Individuals must be in excellent mental health
  • able to understand and sign informed consent
  • available to return for all routine follow-up study visits

Age in the registry: 18 years to 70 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
Brigham and Women's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting

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