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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00434525
Other study ID # 07-011
Secondary ID
Status Completed
Phase Phase 3
First received February 9, 2007
Last updated December 14, 2009
Start date January 2008
Est. completion date December 2009

Study information

Verified date August 2009
Source North Texas Veterans Healthcare System
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

- The investigators aim to determine the clinical and metabolic effects of sleeve gastrectomy with or without omentectomy in the treatment of morbid obesity.

- The investigators hypothesize that the endocrine suppression of ghrelin (appetite hormone)and resistin (insulin antagonist) provided by sleeve gastrectomy and omentectomy (omentum or intra-abdominal fat removal) will provide clinical and metabolic benefits for morbidly obese patients.


Description:

This is a phase 3 prospective randomized trial.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Morbidly obese VETERANS ONLY (BMI>35 with comorbidities or BMI>40)

- Age > 18

Exclusion Criteria:

- Pregnancy

- Uncontrolled medical or psychiatric conditions

- Previous bariatric procedure

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Laparoscopic restrictive procedure
Patients will receive laparoscopic sleeve gastrectomy with or without omentectomy
Sleeve gastrectomy
Sleeve gastrectomy

Locations

Country Name City State
United States VA North Texas Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
North Texas Veterans Healthcare System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight loss 5 years No
Secondary Metabolic outcomes 5 years No
Secondary Diabetes resolution 5 years No
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