Severe Obesity Clinical Trial
Official title:
Surgical Treatment of Severe Obesity by Roux-en-Y Gastric Bypass: a Randomized Prospective Study on the Effect of Reciprocal Changes in Y-limb Lengths on Intestinal Absorption of Dietary Fat, Protein and Carbohydrate.
| NCT number | NCT01252511 |
| Other study ID # | 010-271 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | January 2011 |
| Est. completion date | January 14, 2017 |
| Verified date | January 2016 |
| Source | Baylor Research Institute |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to determine whether or not the length of the biliopancreatic limb of the Roux-en-Y anastamosis plays a critical role in the development of malabsorption after gastric bypass for treatment of severe obesity.
| Status | Completed |
| Enrollment | 20 |
| Est. completion date | January 14, 2017 |
| Est. primary completion date | August 2014 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Patients with severe obesity (BMI equal to or greater than 50) who have been scheduled to receive Roux-en-Y gastric bypass. Exclusion Criteria: - Previous abdominal surgery, chronic diarrhea, and severe constipation. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Baylor University Medical Center | Dallas | Texas |
| Lead Sponsor | Collaborator |
|---|---|
| Baylor Research Institute |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Selective fat malabsorption | To learn how to create an operation resulting in the predominance of fat malabsorption over protein malabsorption. | 1 year after RYGB surgery |
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