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Obesity, Morbid clinical trials

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NCT ID: NCT01098942 Completed - Morbid Obesity Clinical Trials

Bariatric Surgery and Skeletal Health

Start date: November 2009
Phase:
Study type: Observational

Bone loss may occur after bariatric (weight loss) surgery, but standard methods of measuring bone density in obese patients are potentially inaccurate. This study uses quantitative computed tomography to examine changes in bone mineral density after bariatric surgery. We are also studying mechanisms which may explain bone loss after bariatric surgery.

NCT ID: NCT01086722 Completed - Overweight Clinical Trials

Pharmacokinetics in Morbid Obesity After Bariatric Surgery

FAROBE/1
Start date: February 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Morbid obesity (MO) is associated with several disorders such as hypertension, type 2 diabetes, dyslipemia and degenerative arthropathy that require pharmacological treatment. Drug bioavailability and metabolism in patients with MO is altered compared to population controls. Bariatric surgery is the gold standard treatment for MO when conventional therapy fails. Bariatric surgery techniques can modify drug absorption in MO patients. These modifications depend on the drug absorption characteristics and on the bariatric surgery technique used. The changes in weight and body composition caused by BS at middle term can alter drug bioavailability and metabolism. The kinetics of the "normalization" process in patients with MO after bariatric surgery is unknown Objectives. To analyze the changes in drug metabolism and pharmacokinetics. To establish drug dosing criteria in the post-intervention period in patients with MO after bariatric surgery. To determine the relationship between changes in drug bioavailability and metabolism in MO after bariatric surgery (longitudinal gastrectomy and Y-roux gastric by-pass).

NCT ID: NCT01086111 Completed - Type 2 Diabetes Clinical Trials

The Effect of a Gastric Bypass on Type 2 Diabetes in the Morbidly Obese Patient

Start date: February 2010
Phase: N/A
Study type: Observational

Proof of concept, of RYGBP and its capabilities to cure type 2 diabetes (DM 2) and sleep apnea has already been recognized in the reports on weight loss surgery. The investigators project aims to prove that RYGBP also recovers the beta cell function (BCF) Clamp tests, the gold standard for testing IS and BCF, will be performed preoperative and early postoperatively. Aims & methodology: Analysis of the short-term effect of gastric bypass and sleeve gastrectomy on insulin sensitivity and beta cell function. Preoperative baseline insulin sensitivity and beta cell function will be assessed with euglycemic and hyperglycemic clamp tests. These results will be compared with the results of the same tests carried out 3 weeks postoperative. To determine if the duodenal exclusion is causing this effect. The results of the clamp tests 3 weeks postoperative will be compared

NCT ID: NCT01064596 Completed - Obesity Clinical Trials

Fondaparinux Population Pharmacokinetic to Morbid Obese Patients in Post-operatory Bariatric Surgery

Start date: February 2010
Phase: Phase 4
Study type: Observational

After bariatric surgery , thromboembolics complications are major cause of mortality. However, in obese patients, thromboprophylaxia is a controversy. Fondaparinux' efficacy is superior to HBPM, and is a good treatment for this population. Pharmacokinetics information with Fondaparinux in this population are rare.

NCT ID: NCT01063127 Completed - Morbid Obesity Clinical Trials

A Longitudinal Study on Short-term Effects of Gastric Bypass on Glucose Homeostasis in Obesity

Start date: February 2010
Phase: N/A
Study type: Observational

The purpose of this study is to quantify the relative contribution of improved insulin sensitivity and improved insulin secretion to the glycaemic effect of bariatric surgery.

NCT ID: NCT01045499 Completed - Metabolic Syndrome Clinical Trials

LAGB as a Treatment for Morbid Obesity in Adolescents

Start date: September 13, 2005
Phase: N/A
Study type: Interventional

Laparoscopic adjustable gastric banding (LAGB) has been used worldwide to help selected morbidly obese adults to lose weight. The FDA has approved LAGB only for patients 18 years or older. Our hypothesis that LAGB can be used to assist selected adolescents between 14 and 17 years lose weight and that the procedure can be performed safely in this age group. We are also evaluating the effects of weight loss after LAGB on known comorbid conditions such as sleep apnea syndrome and insulin resistance, and also on psychological health.

NCT ID: NCT01042002 Completed - Morbid Obesity Clinical Trials

Effect of Exercise Before Gastric Bypass

Start date: August 2006
Phase: N/A
Study type: Interventional

Exercise training is proved to protect against premature cardiovascular mortality. Additionally there is evidence that relatively high exercise intensity may be an important factor for improving aerobic capacity and endothelial function in patients with post-infarction heart failure, metabolic syndrome, coronary artery disease, as well as in overweight and obese individuals. The aims of this study is to investigate if High-intensity exercise before a gastric bypass operation will decrease hospitalization days and complications after the gastric bypass.

NCT ID: NCT01041131 Completed - Clinical trials for Clinically Severe Obesity

Laparoscopic Revision of Vertical Banded Gastroplasty to Gastric Bypass

VBG
Start date: October 2009
Phase: N/A
Study type: Observational

The main aim of this study is to analyze and report the intermediate term outcomes after laparoscopic revision Roux-en-Y gastric bypass (RYGB) surgery for failed and/or complicated Vertical Banded Gastroplasty (VBG). The foremost outcome measurements are 1) Fat loss mainly measured as weight loss and expressed as trends in BMI, %EWL, and/or %EBL. 2) Trend in Comorbidity status. 3) Subjective Satisfaction and Health-Related Quality of Life "HR-QoL" are measured by a standardized, non-validated satisfaction questionnaire and by a validated, disease-specific worldwide used HR-QoL questionnaire. 4) Morbidity & Mortality include nutritional status and metabolic complications. Consequently, secondary objectives of this study are the following. 1) To assess failure rate defined as percentage of excess weight loss < 50%, lowest BMI >35 for morbidly obese (MO) or >40 for superobese (SO), and/or lack of resolution/improvement of major comorbidities at the point in time when assessed at each postoperative year after the surgery under study. 2) To evaluate the metabolic and nutritional status by measurements of particular clinical and biochemical parameters.

NCT ID: NCT01041105 Completed - Clinical trials for Gastroesophageal Reflux Disease

Gastric Bypass After Previous Anti-reflux Surgery

RYGBafterARS
Start date: December 2008
Phase: N/A
Study type: Observational

The goal of this study is to describe the clinical presentation, indications, and operative treatment as well as assess the morbidity, mortality, and overall performance of revisional Roux-en-Y gastric bypass (RYGB) after either failed or functional antireflux surgery "ARS" in obese patients. With such information, we hope to determine which features might assist us in advancing our knowledge about Gastro-Esophageal Reflux Disease "GERD", the best option for primary ARS, and mechanisms of failure in the obese population as well as in identifying predictors of outcome after revisional surgery in this population.

NCT ID: NCT01040572 Completed - Clinical trials for Clinically Severe Obesity

Laparoscopic Revision Gastric Bypass for Weight Recidivism

WR
Start date: October 2009
Phase: N/A
Study type: Observational

The main aim of this study is to analyze and report traditional, patient-centered, and composite intermediate-term outcomes after laparoscopic revision Roux-en-Y gastric bypass surgery for weight recidivism.