VA North Texas
Dallas, Texas, 75216, United States
NCT Number: NCT00434655
* The investigators aim to determine the clinical and metabolic outcomes of two available bariatric restrictive procedures: laparoscopic adjustable gastric banding (LAP-BAND) and laparoscopic sleeve gastrectomy for the treatment of morbid obesity (BMI > 35 with comorbidities or BMI > 40) in VETERANS. * The investigators hypothesize that the short and long term outcomes between laparoscopic adjustable gastric banding (LAP-BAND) and sleeve gastrectomy are similar in VETERANS.
Looking for future studies?
Notify Me18 year–65 year
All sexes
Interventional
Phase 3
Dallas, Texas, 75216, United States
This is a bariatric surgery Phase 3 prospective trial.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Morbidly Obese VETERANS will receive one of two laparoscopic bariatric restrictive procedures.
Time frame: 5 years
Time frame: 5 years
Time frame: 2 years
Time frame: 5 years
Time frame: 5 years
Looking for future studies?
Notify MeNorth Texas Veterans Healthcare System
Fed
Laparoscopic Adjustable Gastric Banding Versus Laparoscopic Sleeve Gastrectomy: A Prospective Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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