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Clinical Trials/NCT01153308
NCT01153308
Completed
Not Applicable

Outcomes of Bariatric Surgery (UMMMC Bariatric Surgery Registry)

University of Massachusetts, Worcester1 site in 1 country4,785 target enrollmentApril 2005
ConditionsMorbid Obesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Morbid Obesity
Sponsor
University of Massachusetts, Worcester
Enrollment
4785
Locations
1
Primary Endpoint
Weight Loss after surgery
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this registry is to monitor and evaluate the efficacy, as well as safety, of bariatric surgery performed at UMass Memorial Medical Center, including laparoscopic gastric bypass surgery and laparoscopic gastric banding, in the surgical treatment of morbid obesity and associated co-morbidities such as type 2 diabetes, sleep apnea and cardiovascular disease.

Detailed Description

See brief Summary

Registry
clinicaltrials.gov
Start Date
April 2005
End Date
April 2015
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Massachusetts, Worcester
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Must be scheduled for Bariatric Surgery @ UMMMC

Exclusion Criteria

  • Not scheduled for Bariatric Surgery @ UMMMC

Outcomes

Primary Outcomes

Weight Loss after surgery

Time Frame: Preop, Postop, Six Months, and Annually

Baseline weight is recorded preoperatively. Time points after surgery when weight is recorded are two weeks, six weeks, 6 months, 1 year, 18 months, 2 years, then annually on the anniversary date of surgery.

Secondary Outcomes

  • Resolution of Co-morbidities, such as Type 2 Diabetes, Sleep Apnea, Hypertension(Preop, Postop, Six Months, Annually)

Study Sites (1)

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