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Obesity, Morbid clinical trials

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NCT ID: NCT00592202 Completed - Morbid Obesity Clinical Trials

Laparoscopic Adjustable Gastric Banding as a Treatment for Morbid Obesity in Adolescents

Start date: December 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the LAP-BAND system is safe and effective in morbidly obese adolescents.

NCT ID: NCT00590655 Completed - Weight Loss Clinical Trials

Maintenance Programme After Weight Loss

Start date: August 2002
Phase: N/A
Study type: Interventional

The aim of this study is to compare a weight reduction programme with and without a maintenance programme in patients with severe obesity.

NCT ID: NCT00553852 Completed - Obesity Clinical Trials

Replacement GH Therapy After Bariatric Surgery in Patients With Very Severe Obesity

GH&LASGB
Start date: July 2007
Phase: Phase 3
Study type: Interventional

Obesity and obesity-related diseases have reached epidemic proportions in Western countries (1-3). Laparoscopic-adjustable silicone gastric banding (LASGB) is a purely restrictive operation that determine effective weight loss without inducing malabsorption (4-6). However, also after LASGB body weight loss is almost invariably associated with Free Fat Mass (FFM) loss, and the relevance of the FFM contribution to total energy expenditure is well-known (7-8). Different endocrine axes are reported to affect FFM. We previously reported that low levels of DHEA-S, an adrenal steroid with controversial anti-adipogenic and anti-atherogenic effects, are increased after the massive and sustainable weight loss induced by LASGB in severely obese premenopausal women and correlated with the higher post-operative FFM (9-10). It is also well known that GH/IGF-I axis exerts relevant effects on FFM and that reduced GH levels might increase Fat Mass (FM) and reduce FFM (11,12). Morbidly obese patients have a reduced GH secretion, generally reversible after weight loss (13-14). In a recent study currently in press, we reported that a persistent deficiency in the GH/IGF-I axis in very obese females is associated to lower decrease in FM after LASGB. Low IGF-I plasma levels have also been reported to be independent prognostic factors of liver steatosis and non-alcoholic steatohepatitis in morbidly obese patients (15) and ultrasound- measured hepatic left lobe volume might represent a reliable tool for the evaluation of liver involvement in obesity (16). GH deficiency (GHD) in adult patients is associated with an increase in FM and a parallel decrease in FFM (17). The severity of GDH is correlated to cardiovascular risk, body composition abnormalities and bone loss, and decreased left ventricular ejection fraction (18-20). GH therapy has been demonstrated to be effective in normalizing body composition, with beneficial effects up to a 2-years follow-up period (21-24). GH therapy has also been reported to be effective in sparing FFM during weight loss in obese patients and metabolic syndrome (25,26). However, these studies have some limitations due to the duration of the treatment and the lack of a preliminary evaluation of the GH/IGF-I axis secretory status in obese patients before the GH therapy. At present there are no data on the evaluation of the GH/IGF-I status before and after bariatric surgery and the effectiveness of recombinant GH treatment in very severe obese patients.

NCT ID: NCT00543140 Completed - Morbid Obesity Clinical Trials

Post Implantation/Post Market Evaluation of the Swedish Adjustable Gastric Band

SAGB-PM
Start date: August 2006
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the long term safety of the Swedish Adjustable Gastric Band (SAGB) in subjects with an SAGB in place. Specifically it is designed to determine the re-operation rate (band revision, band replacement and explants resulting from serious adverse device-related event {SADE}) of gastric banding at 4 and 5 year post implant.

NCT ID: NCT00535990 Completed - Colorectal Cancer Clinical Trials

Minimally Invasive Surgery (MIS) Database for the Purpose of Research

Start date: September 2007
Phase:
Study type: Observational

The Minimally Invasive Surgery Team (MIST) are establishing a separate research database to find out more about patient's undergoing minimally invasive surgery (laparoscopic , open and robot assisted) procedures at UCSD. The hope is that collection of this information will give physicians a better knowledge and understanding of the benefits of minimally invasive surgery and possibly assist physicians to better manage future patients.

NCT ID: NCT00532896 Completed - Obesity Clinical Trials

Impact of Weight Loss Following Bariatric Surgery on Pulmonary Function in Patients With Morbid Obesity

Start date: April 2006
Phase: N/A
Study type: Observational

Increase in body mass index (BMI)is associated with a decrease in expiratory flows.Obesity is also associated with an increased prevalence of asthma.Consequences of obesity on respiratory function and on bronchial responsiveness are still to be documented. This study aims to evaluate, before and after surgery, the impact of a bariatric surgery (biliopancreatic diversion with duodenal switch)on respiratory function in patients with morbid obesity . Our hypothesis is that weight loss following bariatric surgery will induce significant improvements in pulmonary function and airway responsiveness, and, as a consequence, a reduction in respiratory symptoms,these changes being correlated with a reduction in systemic markers of inflammation. Maintenance of weight loss after one year will permit the persistence of these improvements

NCT ID: NCT00512512 Completed - Morbid Obesity Clinical Trials

Transoral Endoscopic Liver Biopsy During Laparoscopic Gastric Bypass

Start date: June 2007
Phase: N/A
Study type: Observational

This research is being done to evaluate the ability to obtain a liver sample using upper endoscopy rather than through a laparoscopic procedure. The investigators hypothesize that the endoscopic transoral route is as effective as the laparoscopic route.

NCT ID: NCT00508976 Completed - Pain, Postoperative Clinical Trials

Clinical Proposal for the Comparison of Intraperitoneal Anesthetic to Injected Local Anesthetic

Start date: June 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if pre-incisional lidocaine injection, instilled liquid bupivacaine, intra-abdominal aerosolized bupivacaine, or post-operative bupivacaine injection is superior in post-operative pain control in laparoscopic bariatric surgical patients.

NCT ID: NCT00504036 Completed - Morbid Obesity Clinical Trials

Efficacy of Preoperative Intra Gastric Balloon in Morbidly Obese Patients Selected for Gastric By-pass

BIGPOM
Start date: October 2007
Phase: N/A
Study type: Interventional

To demonstrate, during a prospective randomized medico-economic study, in morbidly obese patients (BMI > 45 kg/m²) selected for a laparoscopic gastric by-pass that, in comparison to usual care, a temporary intra-gastric balloon (6 months) decreases medical costs and peri-operative morbidity.

NCT ID: NCT00501085 Completed - Obesity, Morbid Clinical Trials

LAP-BAND AP Early Experience Trial (APEX)

Start date: June 2007
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the LAP-BAND AP System in severely obese patients.