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Obesity, Morbid clinical trials

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NCT ID: NCT00316446 Completed - Morbid Obesity Clinical Trials

Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone Gastric Bypass

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

The purpose of this study is to determine if gastric bypass patients experience hypoventilation in the immediate postoperative period, and to what degree.

NCT ID: NCT00305032 Completed - Clinical trials for Obstructive Sleep Apnea

Effect of Endoscopic Gastric Balloon Insertion on Obstructive Sleep Apnea in Patients With Morbid Obesity

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

To investigate the effect of weight loss by gastric balloon insertion on parameters of obstructive sleep apnea.

NCT ID: NCT00285220 Completed - Morbid Obesity Clinical Trials

Safety and Efficacy of Laparoscopic Truncal Vagotomy for the Treatment of Obesity

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

This two site study will evaluate the safety and effectiveness of laparoscopic truncal vagotomy for the treatment of obesity with baseline study and 18 month post op follow up.

NCT ID: NCT00254072 Completed - Morbid Obesity Clinical Trials

Evaluation of Endostapled Anastomoses for Laparoscopic Gastric Bypass (EEA-LGB)

EEA-LGB
Start date: January 2007
Phase: N/A
Study type: Interventional

Laparoscopic gastric bypass surgery is a common procedure being performed for the treatment of morbid obesity. The procedure consists of a creation of a small gastric pouch and rerouting the small bowel to bypass the stomach and duodenum. There are two anastomoses in this procedure: the gastrojejunostomy and the jejunojejunostomy. Potential complications after gastric bypass include gastrointestinal bleeding and leaks. Gastrointestinal bleeding can occur at any staple line including the gastrojejunostomy. Potential methods for prevention of postoperative gastrointestinal bleeding include oversewing of the anastomosis or the use of a smaller stapler height. We hypothesize that the use of staplers with smaller staple height will significantly result in a lower rate of staple line bleeding and possible leaks.

NCT ID: NCT00247377 Completed - Morbid Obesity Clinical Trials

Laparoscopic Gastric Bypass vs LAP-BAND for Treatment of Morbid Obesity

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

PURPOSE Obesity is a growing problem in the United States. Severe obesity, known as "morbid obesity", is defined as being 100 pounds in excess of ideal body weight. Nonsurgical treatments for morbid obesity include exercise, dietary restriction, behavior modification, and pharmacological intervention. However, it is estimated that most patients undergoing nonsurgical treatments for weight reduction will regain their weight within 2 to 4 years after treatment. According to the NIH consensus conference in 1991, surgery remains the only effective sustained weight loss treatment for morbid obesity. The Roux-en-Y gastric bypass (GBP) is currently considered the gold standard bariatric surgical operation. Mean weight loss following GBP is approximately 65% of the excess body weight during the first 12 to 18 months postoperatively. Long-term weight loss is in the range of 55-70% of excess body weight loss. Recently, the laparoscopic approach to GBP was reported. Wittgrove and colleagues reported their results of 75 patients who underwent laparoscopic GBP and demonstrated significant short-term advantages with comparable weight loss and reversal of comorbidities compared to the open approach. However, GBP might it be done laparoscopic or open approach can potentially be associated with significant morbidity and mortality such as anastomotic leak, pulmonary embolism, bowel obstruction, and postoperative stricture. The FDA recently approved the laparoscopic adjustable banding system (LAP-BAND) for use in the United States in June 2001. The LAP-BAND system is a device designed to induce weight loss in severely obese patients. It is surgically placed around the proximal stomach to create a small proximal stomach pouch and restricted opening, or stoma, through which passage of food will be slowed. An inflatable portion along the inner aspect of the band is connected to an access port, placed intramuscularly. This enabled stoma adjustments to be made without the need for further surgery. The advantages of the LAP-BAND system included no cutting or opening of the stomach wall, ability to adjust the stoma and a technically easier operation to perform than laparoscopic GBP. We wanted to evaluate if the LAP-BAND procedure is as effective as the laparoscopic GBP procedure for treatment of morbid obesity.

NCT ID: NCT00239850 Completed - Morbid Obesity Clinical Trials

Morbid Obesity: Effects of Conservative Treatments and Gastric Bypass Surgery

Start date: August 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of conservative treatments of obesity with surgery (gastric bypass).

NCT ID: NCT00212160 Completed - Obesity Clinical Trials

The Role of the Omentum in the Treatment of Morbid Obesity

Start date: January 2005
Phase: N/A
Study type: Interventional

The purpose of this research is to determine some of the reasons that blood sugar and insulin levels improve after bariatric surgery but before weight loss begins, as well as why people respond differently to weight loss surgery. It will also examine whether removing the fat around the stomach and large intestine (the omentum) will improve weight loss. Finally, it will see why there are differences between Whites and African Americans who have weight loss surgery.

NCT ID: NCT00200083 Completed - Obesity Clinical Trials

Study of Weight Loss Using Gastric Stimulation in Obese Patients

SHAPE
Start date: May 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to test the effect of an implanted device that stimulates the stomach to help obese patients lose weight.

NCT ID: NCT00200018 Completed - Clinical trials for Severe to Morbid Obesity and Type 2 Diabetes

Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Diabetes

ASSIST
Start date: June 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to test the effect of an implanted device that stimulates the stomach on weight loss in patients suffering from obesity and type 2 diabetes.

NCT ID: NCT00166205 Completed - Obesity, Morbid Clinical Trials

Safety and Effectiveness Study of The Swedish Adjustable Gastric Band (SAGB) in the Treatment of Morbid Obesity

Start date: June 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the Swedish Adjustable Gastric Band (SAGB) is safe, and effective in achieving weight loss in patients with Morbid Obesity.