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Terminated Not applicable Interventional Results available

Safety and Efficacy of EndoBarrier in Subjects With Type 2 Diabetes Who Are Obese

ClinicalTrials.gov ID: NCT01728116

Public ClinicalTrials.gov record NCT01728116. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 11, 2026, 4:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Multi-Center, Pivotal Efficacy and Safety Study Comparing the EndoBarrier Gastrointestinal Liner System vs. Sham for Glycemic Improvement in Inadequately Controlled Obese Type 2 Diabetic Subjects on Oral Anti-Diabetes Agents

Study identification

NCT ID
NCT01728116
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Morphic Medical Inc.
Industry
Enrollment
325 participants

Conditions and interventions

Interventions

  • EndoBarrier Device
  • Sham Procedure Procedure

Device · Procedure

Eligibility (public fields only)

Age range
21 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2012
Primary completion
Jan 31, 2016
Completion
Jan 31, 2016
Last update posted
Jan 31, 2017

2012 – 2016

United States locations

U.S. sites
25
U.S. states
21
U.S. cities
23
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Mayo Clinic Arizona Scottsdale Arizona 85259
Little Rock Diagnostic Center (LRDC) Little Rock Arkansas 72205
Cedars-Sinai Medical Center Los Angeles California 90048
Stanford University School of Medicine Stanford California 94305
University of Colorado/ Anschutz Health & Wellness Center Aurora Colorado 80045
Emory University Atlanta Georgia 30303
Northwestern University Chicago Illinois 60208
Kentucky Research Group Louisville Kentucky 40218
Tulane University Health Sciences Center New Orleans Louisiana 70112-2699
MedStar Health Research Institute Hyattsville Maryland 20782
Massachusetts General Hospital Boston Massachusetts 02114
Boston Medical Center Boston Massachusetts 02118
University of Michigan Ann Arbor Michigan 48109
Mayo Clinic Minnesota Rochester Minnesota 55905
Washington University St Louis Missouri 63110
Billings Clinic Billings Montana 59101
Beth Israel Medical Center New York New York 10003
University of North Carolina Chapel Hill North Carolina 27599
Cleveland Clinic Cleveland Ohio 44195
Legacy Research Institute Portland Oregon 97232
Endocrinology Consultants of East Tennessee & Gastrointestinal Associates Knoxville Tennessee 37909
Dallas Diabetes Dallas Texas 75230
UT Southwestern Medical Center Dallas Texas 75390-7170
The Methodist Hospital Research Institute Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01728116, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 31, 2017 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01728116 live on ClinicalTrials.gov.

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