跳至主要内容
临床试验/NCT05711758
NCT05711758招募中不适用

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

Christopher C. Thompson, MD, MSc1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年9月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
30
试验地点
1
主要终点
Weight change compared to baseline

研究概览

简要总结

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.

详细描述

Obesity, defined as body mass index (BMI) greater than 30 kg/m2 in adults, is affecting 30% of the global population and a significant healthcare burden. [1] Obesity has increased dramatically over the last few decades, with over 650 million adults, or 13% of the world's total adult population, diagnosed with the disease in 2016 - a figure that has nearly tripled since 1975.[1] In the U.S the obesity prevalence for U.S. adults increased from 14.1% to 26.7%, or an 89.9% increase between 1993 and 2008.[1,2,3] As a result, current and potential interventions, and treatment strategies to combat obesity have become more important.

The current treatment of obesity involves multiple strategies with combination of non-pharmacologic, pharmacologic, endoscopic, and surgical interventions. There are several FDA-approved pharmacotherapies for the treatment of obesity such as orlistat, phentermine-topiramate, naltrexone-bupropion, liraglutide, and semaglutide. For adults with a body mass index (BMI) of 40 kg/m2 or 35 kg/m2 and obesity-related comorbidity, bariatric surgery can be offered. [4, 5] Endoscopic bariatric and metabolic therapies (EBMT) have emerged as an alternative treatment for patients with obesity with a BMI over 30kg/m2 or 27 kg/m2 with an obesity-related comorbidity. The interest in EBMT is growing given their safety, efficacy, and non-invasive nature. Current FDA-cleared devices that can be used for EBMT include intragastric balloons and suturing devices for endoscopic sleeve gastroplasty (ESG). Additionally, a variety of Endo surgical knifes are approved for tissue dissection such as myotomy.

Gastric interventions used to treat obesity work by interfering with gastric accommodation, breakdown and mixing of food, or gastric emptying. Delaying gastric emptying was shown to be a major mechanism of action for both ESG and IGB which is also correlated with weight loss [6].

Antral peristalsis constitutes an important mechanism for gastric emptying. The antrum also serves as a food sensor which needs to be filled to a certain level before food is pumped into the duodenum. [7] Therefore, targeting the antrum is a feasible strategy to delay gastric emptying, induce satiety, and promote weight loss.

In fact, one of the recently FDA-cleared EBMT devices, the Transpyloric Shuttle (Baronova, MA), focuses on inhibiting the antral pump as its primary mechanism of action. This device consists of two interconnected large and small bulbs, positioned in the antrum and duodenum respectively, that cause intermittent obstruction of the pylorus, leading to a delay in gastric emptying (10).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • untreated H. pylori infection
  • gastroparesis
  • active smoking
  • an ongoing or a history of treatment with opioids in the last 12 months prior to enrollment
  • previous pyloromyotomy or pyloroplasty
  • gastrointestinal obstruction
  • severe coagulopathy
  • esophageal or gastric varices and/or portal hypertensive gastropathy
  • pregnancy or puerperium
  • 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)
  • lactation
  • history of gastrointestinal surgery
  • any serious health condition unrelated to their weight that would increase the risk of endoscopy
  • chronic abdominal pain
  • active psychological issues preventing participation in a lifestyle modification program
  • a known history of endocrine disorders affecting weight (uncontrolled hypothyroidism)
  • an inability to provide informed consent
  • use of any medication that may interfere with weight loss
  • use of any medication that may interfere with gastric emptying
  • any other condition which the investigator may deem as an impediment to compliance or hinder completion of the proposed study

研究组 & 干预措施

PSAM Treatment Patients with no prior endoscopic bariatric therapies

Subjects with no prior endoscopic bariatric therapies having esophagogastroduodenoscopy (EGD) with Pylorus Sparing Antral Myotomy (PSAM) with standard of care lifestyle modification therapy.

干预措施: PSAM Treatment Patients (Procedure)

PSAM Treatment Patients with prior primary endoscopic bariatric therapies

Subjects with prior primary endoscopic bariatric therapies having esophagogastroduodenoscopy (EGD) with Pylorus Sparing Antral Myotomy (PSAM) with standard of care lifestyle modification therapy.

干预措施: PSAM Treatment Patients (Procedure)

PSAM Treatment Patients with prior revision endoscopic bariatric therapies

Subjects with prior revision endoscopic bariatric therapies having esophagogastroduodenoscopy (EGD) with Pylorus Sparing Antral Myotomy (PSAM) with standard of care lifestyle modification therapy.

干预措施: PSAM Treatment Patients (Procedure)

结局指标

主要结局

Weight change compared to baseline

时间窗: Screening, Procedure day, 1 month, 3 month, 6 month, 9 month, 12 months

Percent total body weight loss

Adverse Events

时间窗: Procedure day, 1 month, 3 month, 6 month, 9 month, 12 months

Changes to health compared to baseline

Change in tolerability from procedure day to 12 months

时间窗: Procedure day, 1 month, 3 month, 6 month, 9 month, 12 months

How the subjects feel after the procedure based on pain scale and AE's

次要结局

  • Ghrelin levels compared to baseline(Screening, 6 months, 12 months)
  • Change in Quality of Life compared to baseline(Screening, 1 month, 3 month, 6 month, 9 month, 12 months)
  • Insulin levels compared to baseline(Screening, 6 months, 12 months)
  • Gastric Emptying compared to baseline(Screening, 6 months, 12 months)
  • Glucose levels compared to baseline(Screening, 6 months, 12 months)
  • Physiologic Changes of gastric motility/transit compared to baseline(Screening, 6 months, 12 months)
  • Gastric Motility compared to baseline(Screening, 1 month)
  • HgA1c levels compared to baseline(Screening, 6 months, 12 months)
  • HOMA-IR blood plasma levels compared to baseline(Screening, 6 months, 12 months)

研究者

发起方
Christopher C. Thompson, MD, MSc
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Christopher C. Thompson, MD, MSc

Director of Endoscopy

Brigham and Women's Hospital

研究点 (1)

Loading locations...

相似试验