Transoral Gastric Volume Reduction as an Intervention for Weight Management

Obesity Clinical Trial

Official title: Transoral Gastric Volume Reduction as an Intervention for Weight Management

Status Withdrawn

Clinical Trial Summary

This study assesses weight loss from the Endoscopic Vertical Gastroplasty or Fogel Gastroplasty (FG). The purpose of the study is to:

• Document that weight loss occurs (12 months)

• Determine if it alters general wellbeing (emotionally and physically)

Clinical Trial Description

This will be a prospective study evaluating the percentage of weight loss in patients that have undergo the Endoscopic Vertical Gastroplasty or Fogel Gastroplasty (FG). Fogel's Gastroplasty is a procedure where The subject will be placed under general anesthesia in accordance with the Institution's standard practice. The procedure will last approximately 1-2 hours. Following induction of anesthesia, the overtube will be placed, a gastroscope will be inserted to examine esophageal and gastric anatomy and re-confirm there are no anatomical contraindications to the procedure. The gastroscope will also be used to record images of the stomach prior to insertion of the OverStitch. Once the examination is complete the gastroscope will be removed. The OverStitch system will then be inserted orally to the per-operative site. CO2 will be used rather than air for the insufflation that is required during the procedure to minimize abdominal distention. The physician will place an interrupted suture pattern in a manner which partitions the greater curvature of the stomach from the Angle of His to the level of the incisura, creating a tube-like passage for gastric volume reduction. Afterwards, the remaining gastric volume will be reduced using a circumferential running stitch. Once complete, the OverStitch system will be removed and a standard gastroscope will be inserted to record post procedure endoscopic images.

Anthropometric measurements as Weight, Height, BMI and Waist Circumference will be collected at Baseline, 3, 6 and 12 months after procedure ;

Related Conditions & MeSH terms

• Body Weight
• Obesity
• Overweight
• Weight Loss

• NCT number: NCT02578836
• Study type: Interventional
• Source: University of Miami
• Status: Withdrawn
• Phase: N/A
• Start date: August 1, 2017
• Completion date: November 2018