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Clinical Trials/NCT05750134
NCT05750134Not yet recruitingNot Applicable

Endoscopic Sleeve Gastroplasty for Overweight or Moderately Obese Patients: Identification of Predictive Factors for Weight Loss

Assistance Publique - Hôpitaux de Paris1 site in 1 country105 target enrollmentStarted: March 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
105
Locations
1
Primary Endpoint
Serum metabolite profile using widely targeted metabolomics according to weigh loss amount (less than 10% of total weight versus more than 10% of total weight loss at 12 months post-surgery)

Study Overview

Brief Summary

Weight loss is of paramount importance to ameliorate obesity-related complications. Endoscopic sleeve gastroplasty is a new therapeutic option to obtain significant weight reduction in obese patients. Nevertheless, a only a part of patients experience sufficient weight loss to improve comorbidities. A better understanding of mechanisms driving body weight trajectory after endoscopic sleeve gastroplasty may help patient selection and improve efficacy. The main aim of this study is to identify factors associated with weight reduction after endoscopic sleeve gastroplasty in patients with overweight or morbid obesity without indication to bariatric surgery. For this purpose, the investigators conduct a retro-prospective cohort study including patients with overweight or moderate obesity undergoing endoscopic sleeve gastroplasty between March 2017 and March 2023

Detailed Description

The prevalence of obesity is increasing worldwide, and it is estimated that one quarter of the world's population will be overweight or obese by 2045. Obesity can lead to complications, including cardiovascular damage (myocardial ischemia and stroke), liver damage (non-alcoholic steatohepatitis and liver cancer), diabetes and extra-hepatic cancers. In this context, achievement of a significant long-term weight loss is of paramount importance to ameliorate patient outcome. Bariatric surgery is the most effective treatment for severe obesity and results in a significant long-term weight loss. However, bariatric surgery is restricted to patients with a BMI >40 kg/m2 or >35 kg/m2 with commodities (hypertension, diabetes, sleep apnoea, NASH). Therefore, the majority of obese patients do not benefit from this procedure. Recent advances in flexible endoluminal endoscopy now provide the tools for transoral endoscopic gastric volume reduction (ESG, endoscopic sleeve gastroplasty). The gastric body is reduced by an endoscopic procedure involving suture plications. This minimally invasive method may be a good therapeutic option to obtain a significant weight reduction in patients with moderate obesity or those with severe obesity and no indication for bariatric surgery (BMI between 35 and 40 kg/m2 without commodities). In this context this study aims to identify predictive factors of weight loss following ESG and explore changes of metabolic parameters, metabolomic profiles and gut microbiota profiles. This is a retro-prospective cohort study including patients with moderate obesity undergoing ECG between March 2017 and September 2023. Clinical parameters (weight, high, BMI, weight fluctuations), serum metabolic parameters (standard lipid profile, lipoprotein levels, fasting plasma glucose, insulin levels, C-peptide levels, hemoglobin A1c) and liver function test parameters (standard biology, transient elastometry, Fibrotest®, Actitest®, abdominal ultrasound) are systematically collected for all patients before ESG and then at three- and twelve-month post-ESG. Samples of serum, plasma, stools and saliva are also systematically collected for research purpose before ESG and then at three- and twelve-month post-ESG. Each sample is stored at -80°C for subsequent analysis. Metabolomic/lipidomic analysis will be used to quantify metabolite and lipid species in serum/plasma samples. Metagenomic analysis will be used to characterise faecal and salivary microbiota profiles.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Other

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age ≥18 years
  • Patients giving their consent for the study
  • Body mass index between 28 and 35 kg/m2 with co-morbid condition (type 2 diabetes, hypertension, dyslipidemia, obstructive sleep apnea, non-alcoholic fatty liver disease or invalidating joint pain)
  • No weigh loss following life-style changes

Exclusion Criteria

  • Antibiotic treatment during the three previous months
  • Patients at risk of gastric cancer requiring regular endoscopic surveillance
  • Gastric localization of Crohn disease
  • Portal hypertension
  • Severe hepatic or renal failure
  • Ongoing peptic ulcer
  • Severe associated disease
  • History of previous bariatric surgery

Outcomes

Primary Outcomes

Serum metabolite profile using widely targeted metabolomics according to weigh loss amount (less than 10% of total weight versus more than 10% of total weight loss at 12 months post-surgery)

Time Frame: Before endoscopic sleeve gastroplasty

A volume of 50 µl of serum/plasma will be used for analysis of serum metabolites using widely targeted metabolomics mass spectrometry.

Secondary Outcomes

  • Basic serum lipid profile at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Liver function test parameter Alanine transaminase (ALT) at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Liver function test parameter Alkaline phosphatase (ALP) at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Serum metabolites using widely targeted metabolomics at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • C peptide at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Liver function test parameter Gamma-glutamyltransferase (GGT) at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Insulin at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Ferritin at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Clinical parameters at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Glycated hemoglobin at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Liver function test parameter aspartate transaminase (AST) at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Liver fibrosis assessed by transient elastometry at baseline and then at 3 and 12 month post-intervention(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Liver steatosis assessed by controlled attenuation parameter (CAP) at baseline and then at 3 and 12 month post-intervention.(Change from baseline (before endoscopic sleeve gastroplasty) to Month 3 and Month 12)
  • Complications of endoscopic sleeve gastroplasty(During the first week post-endoscopic sleeve gastroplasty and at Month 3 and Month 12)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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