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Study details
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Randomized Trial on Transoral Outlet Reduction and Lifestyle Changes for Weight Regain After Gastric Bypass

Boston Scientific Corporation
NCT IDNCT07015424ClinicalTrials.gov data as of Apr 2026
Target enrollment

108

Study length

about 2.8 years

Ages

18+

Locations

9 sites in CA, FL, IL +3

Why this study is shown

Matches obesityActively enrolling

What this study is about

This trial is testing if a procedure called TORe, combined with lifestyle changes, helps people regain weight after gastric bypass surgery compared to just lifestyle changes alone. Participants will be randomly assigned to either receive the TORe procedure along with intensive lifestyle modifications or only undergo intensive lifestyle changes.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Participate in Intensive lifestyle modification
  • 2.Use TORe with OverStitch

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Total Body Weight Loss

Secondary: Change in 36-Item Short Form Survey (SF-36) Quality of Life Questionnaire, Change in A1C, Change in Alanine transaminase (ALT), Change in Aspartate aminotransferase (AST), Change in Impact of Weight on Quality of Life (IWQOL LITE-CT) Quality of Life Questionnaire, Change in Triglycerides, Number of device and procedure-related Adverse Events (AEs) and Serious Adverse Events (SAEs)

Body systems

Endocrinology