Multi-Center Pre-Bariatric Weight Loss Study
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT00469391 |
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Recruitment Status :
Completed
First Posted : May 4, 2007
Results First Posted : December 30, 2016
Last Update Posted : February 15, 2017
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Obesity | Device: GI Sleeve Implantable weight loss device (EndoBarrier) Procedure: Sham Procedure | Phase 2 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 56 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Treatment |
| Official Title: | A Multi-Center, Pilot Efficacy Study of the GI Sleeve for Pre-Surgical Weight Loss |
| Study Start Date : | June 2007 |
| Actual Primary Completion Date : | October 2008 |
| Actual Study Completion Date : | October 2008 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: GI Sleeve
medical device that mimics gastric bypass mechanism for weight-loss
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Device: GI Sleeve Implantable weight loss device (EndoBarrier)
device for weight loss
Other Name: endobarrier |
| Sham Comparator: Sham Control |
Procedure: Sham Procedure
Weight loss
Other Name: Sham |
- Percent Excess Weight Loss (%EWL) at Week 12 [ Time Frame: 3 months ]Excess Weight Loss was calculated using the Metropolitan Life Table (MET method)
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 55 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- BMI > 35 with a significant comorbid condition or BMI 40-60
- Candidate for Bariatric Surgery
Exclusion Criteria:
- No pathologies of the GI Tract
- No anti-coagulant or non-steroidal anti-inflammatory medications
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00469391
| United States, Florida | |
| Cleveland Clinic Florida | |
| Weston, Florida, United States, 33331 | |
| United States, Massachusetts | |
| Lahey Clinic Medical Center | |
| Burlington, Massachusetts, United States, 01805 | |
| United States, New Hampshire | |
| Dartmouth-Hitchcock Medical Center | |
| Lebanon, New Hampshire, United States, 03756 | |
| United States, North Carolina | |
| Carolinas Medical Center | |
| Charlotte, North Carolina, United States, 28232 | |
| Study Director: | Michael Tarnoff, MD | Tufts Medical Center |
| Responsible Party: | GI Dynamics |
| ClinicalTrials.gov Identifier: | NCT00469391 |
| Other Study ID Numbers: |
06-3 |
| First Posted: | May 4, 2007 Key Record Dates |
| Results First Posted: | December 30, 2016 |
| Last Update Posted: | February 15, 2017 |
| Last Verified: | December 2016 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Plan Description: | De-identified individual patient data is on file at the Sponsor |
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Weight Reduction |
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Weight Loss Body Weight Changes Body Weight |

