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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00790309
Other study ID # NNA-Early DM Resolution
Secondary ID
Status Completed
Phase N/A
First received November 11, 2008
Last updated April 20, 2017
Start date December 2008
Est. completion date February 2017

Study information

Verified date April 2017
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective is to compare inflammatory, hormonal, and metabolic changes in the very short term after various bariatric surgical procedures (Roux-en Y Gastric Bypass, Vertical Sleeve Gastrectomy, and Adjustable Gastric Banding)and other abdominal surgeries, as well as to compare these changes to diet-induced changes in the same population.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria for surgery groups:

- BMI of 30 kg/m2 or higher

- Ages 18-65

- History of impaired glucose tolerance or T2DM

Inclusion Criteria for normal weight group:

- BMI of 30 kg/m2 or lower

- Ages 18-65

Exclusion Criteria:

- Development of an intercurrent infection

- Prior gastric, duodenal, proximal jejunal surgery or pancreas resection

- Current use of thiazolidinediones

- Current use of dipeptidyl peptidase-IV inhibitors (e.g., sitagliptin) or glucagon-like peptide-1 analogs (e.g., exenatide)

- Any condition felt by the PI or co-investigators to interfere with ability to complete the study

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Weight loss surgery
Weight loss surgery
Laparoscopic abdominal surgeries
laparoscopic abdominal surgeries

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Vanderbilt University Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary Determine to what extent improvements in glycemic control can be attributed to caloric restriction after weight loss surgery 10 days post-op
Secondary Determine changes in inflammatory markers after weight loss surgery 10 days post-op
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