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Obesity, Morbid clinical trials

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NCT ID: NCT02129296 Recruiting - Weight Loss Clinical Trials

Intragastric Balloon, Air Versus Fluid Filled: Randomized Prospective Study

Start date: September 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Gastric balloons are an evolving way of reducing weight. There are two types on the market, up to date. Air filled balloons seem to be more safe, and more tolerable.

NCT ID: NCT02128178 Recruiting - Pulmonary Embolism Clinical Trials

Laparoscopic Bariatric Surgery: Two Regimens of Venous Thromboprophylaxis: Prospective Randomized Study

Start date: November 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Obese patients undergoing bariatric surgery warrant VTE prophylaxis because they are at high risk for developing a fatal pulmonary embolism or postthrombotic syndrome. However, a consensus does not exist on the most effective prophylactic approach.

NCT ID: NCT02128165 Recruiting - Morbid Obesity Clinical Trials

Effect of Gastric Balloon in Morbid Obesity: Prospective Study

Start date: August 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to compare the efficacy of gastric balloon in weight reduction among two different categories of morbidly obese people.

NCT ID: NCT02118844 Recruiting - Morbid Obesity Clinical Trials

Laparoscopic Bariatric Surgery: Impact of Deep Neuromuscular Block on Surgical Conditions

BaChiBloPro1
Start date: July 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether deep neuromuscular blockade compared to moderate neuromuscular blockade may improve the surgical conditions in patients undergoing laparoscopic bariatric surgery.

NCT ID: NCT02085369 Recruiting - Obesity, Morbid Clinical Trials

Effect of Bariatric Surgery on Cognition, Genetics and Lifestyle

Start date: January 2014
Phase:
Study type: Observational

Obesity bariatric surgery patients usually lose more than 50% of their former obesity within a relatively short time (~ 2 years). There is still a lack of knowledge about underlying psychological and biological mechanisms of decline in body weight. The intention of this project is to investigate whether bariatric surgery is associated with patients' cognitive ability, lifestyle and/or gene expression and metabolomics.

NCT ID: NCT02077517 Recruiting - Morbid Obesity Clinical Trials

Stapled vs Hand Sewn Anastomosis in Roux en Y Gastric Bypass for Morbid Obesity: Randomized Clinical Trial

STAVHAS
Start date: January 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare postoperative complications between hand sewn and stapled anastomosis after performing Roux en Y-Gastric Bypass as a treatment for morbid obesity.

NCT ID: NCT02076880 Recruiting - Type 2 Diabetes Clinical Trials

SLEEVEDIAB To Explore the Early and Late Metabolic Effects of Sleeve Gastrectomy in Obese Patients

SLEEVEDIAB
Start date: November 2013
Phase: N/A
Study type: Interventional

Sleeve gastrectomy is a restrictive procedure based on the removal of a large part of the gastric fundus. According to a recent randomized study, weight loss and resolution of diabetes are comparable to that obtained after gastric by-pass (79.7 % versus 80.3%), but with a lower morbidity. The mechanisms involved in the rapid resolution of diabetes after sleeve gastrectomy remain poorly understood, as no specific study in patients with type 2 diabetic obese are available. An increase in post- absorptive levels of Glucagon-like Peptide 1(GLP-1), Peptide YY(PYY) and insulin has been reported, but in non-diabetic subjects mostly. The important caloric restriction in the early postoperative period indeed improves hepatic insulin resistance, regardless of weight loss. Specific metabolic and hormonal effects of this surgical procedure cannot be excluded.The aim of our study is to explore the early and late metabolic effects of sleeve gastrectomy in severely obese patients with non-insulin-treated type 2 diabetes. We will also evaluate insulin sensitivity, insulin secretion and incretin effect. We will include 14 obese patients with type 2 diabetes, considered eligible to bariatric surgery according to HAS criteria, and whose diabetes treatment involves only metformin, sulfonylurea and glinides. They will be randomized to a 1-week caloric restriction period or no caloric restriction, immediately before surgery. Test meals with dosages of blood glucose, insulin, C-peptide, adiponectin, leptin, GLP-1, PYY and ghrelin will be performed before and after caloric restriction, and 1 week, 3 month, 6 month and 12 month after surgery.

NCT ID: NCT02033577 Recruiting - Severe Obesity Clinical Trials

Effects of Long Biliopancreatic Limb Versus Long Alimentary Limb in Superobesity, a Randomized Study

BMI>50
Start date: August 2011
Phase: N/A
Study type: Interventional

Surgical bypassing of a longer section of the small bowel (when doing a gastric bypass operation) gives better results on body weight in the superobese. We do not yet know whether it is beneficial to exclude more of the proximal small bowel or more of the distal. Side effects of bypassing can also be different. Study aims at clarifying possible differences in effects and side-effects of these two surgical-technical variations.

NCT ID: NCT02024542 Recruiting - Morbid Obesity Clinical Trials

Metabolic Responses to Bariatric Surgery

Start date: February 2011
Phase:
Study type: Observational

Research the genetic and biomechanical markers of human adipose tissue on patients with morbid obesity. Additional tissue/fluid collection is also gathered during the time of surgery.

NCT ID: NCT02017314 Recruiting - Morbid Obesity Clinical Trials

VAS Correlation With BMI

Start date: November 2013
Phase: Phase 4
Study type: Interventional

The aim of the study is to observe if any correlation between Body mass index and VAS values exists in patients who has gone under abdominal surgery. Group I : Patients with BMI<30 Group II: Patients with BMI between 30 and 34.9 Group III: Patients with BMI between 35 and 39.9 Group IV: Patients with BMI between 40 and 49.9 Group V : Patients with BMI >50 After the end of surgery patients will be extubated and in the recovery room morphine PCA (patient-controlled analgesia) treatment will be started according to their adjusted body weight. When VAS values over 4,10 mg/kg Paracetamol IV will be used as an escape treatment. VAS values and Delivery and Demand of the PCA and additional need for analgesics will be recorded in the first 48 hours.