Evaluation of Nutritional Interventions to Limit Gestational Weight Gain in Women With Class III Obesity (BMI >40)
NCT07828743
Body Weight, Body Weight Changes
Birmingham, Alabama, United States
View Trial DetailsNCT Number: NCT01026181
This is a prospective case series study; all morbidly obese patients that need surgical management in Royal Alexandra Hospital will be provided 3 surgical options: Laparoscopic Sleeve Gastrectomy (LSG), laparoscopic Roux-en-Y gastric bypass (LR-en-Y), and laparoscopic gastric banding (LGB), safety and effectiveness will be compared among the 3 groups. The outcome measures will be percentage of excess weight loss, BMI, operative time, hospital stays, complications and improvement of comorbidities.
Looking for future studies?
Notify Me18 year–65 year
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: baseline to 2-year postoperation
Change of body weight in Kilograms measured at follow-up visits two year after surgery
Time frame: from baseline to 2-year postoperation
Patients' weight and height were measured at follow up visit 2 years post operation.
BMI was calculated using the formula: weight (kg)/height(meter)^2
Looking for future studies?
Notify MeUniversity of Alberta
Other
Phase II Study of Comparing Outcomes of Laparoscopic Sleeve Gastrectomy, Laparoscopic Roux-en-Y Gastric Bypass and Laparoscopic Gastric Banding to Treat Morbid Obesity
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