Outcomes of Bariatric Surgery/UMMMC Bariatric Surgery Registry
- Conditions
- Morbid Obesity
- Interventions
- Other: Observational Study
- Registration Number
- NCT01153308
- Lead Sponsor
- University of Massachusetts, Worcester
- 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
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 4785
- Must be scheduled for Bariatric Surgery @ UMMMC
- Not scheduled for Bariatric Surgery @ UMMMC
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Bariatric Surgery Patients Observational Study Bariatric Surgery patients at UMass Memorial Medical Center
- Primary Outcome Measures
Name Time Method Weight Loss after surgery 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 Outcome Measures
Name Time Method Resolution of Co-morbidities, such as Type 2 Diabetes, Sleep Apnea, Hypertension Preop, Postop, Six Months, Annually Preoperatively co-morbidities of morbid obesity are recorded as well as treatment (ie: medications, CPAP machine). Resolution of co-morbidities postoperatively is measured/recorded for example by blood tests, sleep study, as well as changes or discontinuation of medications \&/or interventions.
Trial Locations
- Locations (1)
UMass Memorial Medical Center
🇺🇸Worcester, Massachusetts, United States