MedTrace Logo

Assessment of Gastric Volume Reduction in Surgical Weight Loss Candidates

NCT00721227 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2010-09-08

Study results available
· View outcomes & findings →

Summary

This trial will assess the feasibility of reduction gastroplasty with standard suture in bariatric patients who are candidates for surgical weight loss intervention.

Conditions

Interventions

PROCEDURE

Reduction Gastroplasty

* Subjects will undergo reduction gastroplasty by gastric plication * Subjects are followed for 12 months to evaluate outcomes and potential complications.

Sponsors & Collaborators

  • Ethicon Endo-Surgery

    lead INDUSTRY

Principal Investigators

  • Philip R Schauer, M.D · The Cleveland Clinic

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2010-03-31
Completion
2010-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00721227 on ClinicalTrials.gov