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Obesity, Morbid clinical trials

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NCT ID: NCT00998465 Completed - Obesity Clinical Trials

Hemodynamics, Salt Sensitivity and Body Composition in Patients With Morbid Obesity

Start date: November 2009
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the effect of high vs. low sodium intake on blood pressure and system hemodynamics in patients with morbid obesity and to evaluate the impact of laparoscopic gastric bypass on blood pressure, salt sensitivity and body composition in morbidly obese patients. Furthermore, we wants to describe the hemodynamic mechanisms involved in the amelioration of blood pressure during long-term weight loss.

NCT ID: NCT00981500 Completed - Morbid Obesity Clinical Trials

Glucose Homeostasis Pre and Post Bariatric Surgery

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Start date: December 2009
Phase:
Study type: Observational

The investigators wish to study the effects of three forms of bariatric surgery: Roux-en-Y gastric bypass, Sleeve Gastrectomy, and Gastric Banding. The surgery is not part of the clinical trial. If your insurance does not cover the procedure, then you are responsible for payment of the surgical process. We are doing pre and post surgery testing to provide a better understanding of the effect of bariatric surgery-induced weight loss on metabolic function.

NCT ID: NCT00960843 Completed - Morbid Obesity Clinical Trials

Six-month Study to Compare the Effects of Volume- and Pressure-Guided Adjustments on Weight Loss and Satiety

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of this protocol is to determine how band fill volumes that are based on intraband pressure readings can influence the comfortability of the band and to compare weight loss with this methodology to weight loss with the conventional approach recommended in existing product labeling.

NCT ID: NCT00960765 Completed - Clinical trials for Diabetes Mellitus, Type 2

Endotoxin and Intestinal Flora Before and After Gastric Bypass or Banding in Diabetics

Start date: August 2009
Phase: N/A
Study type: Observational

This research project is designed to investigate endotoxin (a toxin present in the wall of certain kinds of bacteria) levels and the type of bacteria present in the intestine before and after Roux-en-Y gastric bypass or gastric banding surgery in patients that meet the classification for morbid obesity (body mass index >40 kg/m2) and type 2 diabetes. It is known that the type of bacteria present in the intestines of normal weight and obese individuals are different, and it is also known that people with obesity and type 2 diabetes have higher levels of endotoxin. It has been shown that the bacteria change over the long run after Roux-en-Y gastric bypass surgery, but the short-term effects are not known and the endotoxin levels after this procedure have never been studied.

NCT ID: NCT00957957 Completed - Obesity, Morbid Clinical Trials

Gut Hormone Profiling in Obese Patients With Type 2 Diabetes (MK-0000-134)

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

This study will examine changes in various gut-derived hormones in obese type 2 diabetic patients before and after elective bariatric surgery.

NCT ID: NCT00951093 Completed - Morbid Obesity Clinical Trials

Gastroesophageal Reflux Disease (GERD) Before and After Gastric Bypass

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

The hypothesis of this study was that gastric bypass (GBP) ameliorates gastroesophageal reflux disease (GERD) in morbidly obese patients.

NCT ID: NCT00948246 Completed - Morbid Obesity Clinical Trials

European Union (EU) Post-Market Study on Easyband®

Start date: April 2009
Phase: N/A
Study type: Observational

The purpose of this study is to collect additional safety, performance and effectiveness data of the Easyband gastric band medical device in the treatment of morbid obesity in 4 European countries where the device is a CE marked approved product.

NCT ID: NCT00923260 Completed - Metabolic Syndrome Clinical Trials

Omentectomy and Metabolic Syndrome

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

The aim of the present study was to evaluate the additional effect of sudden visceral fat reduction by omentectomy on Metabolic Syndrome, acute phase reactants and inflammatory mediators in patients with morbid obesity undergoing Laparoscopic Roux-en-Y Gastric Bypass.

NCT ID: NCT00911989 Completed - Morbid Obesity Clinical Trials

Laparoscopic Sleeve Gastrectomy With Endoscopic Visualization

Start date: July 2009
Phase: N/A
Study type: Interventional

The main objective of this trial is to evaluate endoscopic visualization during a laparoscopic sleeve gastrectomy (LSG) procedure using an endoscope inserted transvaginally through a new device called a Steerable Flex Trocar (SFT).

NCT ID: NCT00905502 Completed - Morbid Obesity Clinical Trials

Intraoperative Fluid Management in Laparoscopic Bariatric Surgery

Start date: April 2007
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the effects of 'high' versus 'low' volume intraoperative fluid administration (Ringer Lactate, RL) on intra- and postoperative parameters, in obese patients undergoing laparoscopic bariatric surgery (i.e., gastric bypass), in order to establish evidence-based data for perioperative fluid management in this patient population. Based on their experience as well as several reports in the literature, the investigators hypothesized that a restrictive approach to intraoperative hydration will reduce the incidence of postoperative complications and the recovery time of gastrointestinal (GI) function, and shorten hospital stay.