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Obesity, Morbid clinical trials

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NCT ID: NCT02148692 Completed - Surgery Clinical Trials

Protective Ventilation With Higher Versus Lower PEEP During General Anesthesia for Surgery in Obese Patients

PROBESE
Start date: July 2014
Phase: N/A
Study type: Interventional

Postoperative respiratory failure, particularly after surgery under general anesthesia, adds to the morbidity and mortality of surgical patients. Anesthesiologists inconsistently use positive end-expiratory pressure (PEEP) and recruitment maneuvers in the hope that this may improve oxygenation and protect against postoperative pulmonary complications (PPCs), especially in obese patients. While anesthesiologists tend to use PEEP higher than in non-obese patients. While it is uncertain whether a strategy that uses higher levels of PEEP with recruitment maneuvers truly prevents PPCs in these patients, use of higher levels of PEEP with recruitment maneuvers could compromise intra-operative hemodynamics. The investigators aim to compare a ventilation strategy using higher levels of PEEP with recruitment maneuvers with one using lower levels of PEEP without recruitment maneuvers in obese patients at an intermediate-to-high risk for PPCs. We hypothesize that an intra-operative ventilation strategy using higher levels of PEEP and recruitment maneuvers, as compared to ventilation with lower levels of PEEP without recruitment maneuvers, prevents PPCs in obese patients at an intermediate-to-high risk for PPC.

NCT ID: NCT02144597 Completed - Morbid Obesity Clinical Trials

Low-calorie Diet and Body Composition Prior to Roux-en-Y Gastric Bypass

LCD
Start date: August 2011
Phase: N/A
Study type: Interventional

Losing weight before undergoing Roux-en-Y gastric bypass (RYGB) surgery may reduce liver fat content and size thereby improving surgical outcomes. This study aims to investigate whether a 2-week or 6-week pre-operative liquid formula low-calorie diet (LCD) reduces liver fat further than a conventional food diet prior to RYGB using magnetic resonance imaging (MRI). The hypothesis is that the 2-week and 6-week liquid formula LCD will reduce liver fat further than the conventional food pre-operative diet.

NCT ID: NCT02144545 Recruiting - Obesity, Morbid Clinical Trials

Impact of Size of Gastric Sleeve on the Weight Loss. Correlation With Gastric Function and Endocrine-metabolic Changes.

Start date: October 2013
Phase: N/A
Study type: Interventional

Morbid Obesity (MO) is considered the most important epidemic in the developed world in the twenty-first century. After initial assessment of morbidly obese patients and the exclusion of potentially correctable causes, management involves a combination of dietary changes, cognitive therapy, physical activity, psychological support and pharmacological treatment. However, any combination of these factors has proven long-term effectiveness in achieving significant and sustained reduction of excess weight. Currently, surgery is the only treatment capable of achieving this goal, interacting also with significant improvement in quality of life and overall long-term mortality. In recent years, several authors have reported excellent short-term results with performing sleeve gastrectomy, but whether some aspects regarding the variability of gastric tubulization design could influence the results obtained in relation to weight loss and functional changes and gastric hormones. The main objective of this study is to assess the size of the gastric tubulization (based probe calibration and the distance from the pylorus to which initiate gastric section) that can provide a better clinical outcome (such as excess weight loss) in patients undergoing surgery for morbid obesity. Secondary objectives were to assess the morphological changes, physiological and hormonal obtained according to the size of the gastric tubulization and its effect on weight loss patients.

NCT ID: NCT02142660 Completed - Severe Obesity Clinical Trials

Sprayshield as Adhesion Barrier System for Obese Patients

Sprayshield
Start date: January 2012
Phase: N/A
Study type: Observational

The application of SprayShield during a laparoscopic band removal (first surgical step) will be evaluated to see if the postoperative adhesions between the stomach, the left liver and the diaphragm are not severe, facilitating the surgical surgical step of a gastric bypass or a sleeve gastrectomy.

NCT ID: NCT02142257 Active, not recruiting - Obesity Clinical Trials

Comparison of Gastric Bypass and AspireAssist Aspiration Therapy for Treatment of Morbid Obesity

Start date: May 2014
Phase:
Study type: Observational

The purpose of this study is to compare Gastric Bypass and AspireAssist Aspiration Therapy over 5 years of treatment with regards to weight loss, quality of life, complications, adverse events, and health economics.

NCT ID: NCT02137330 Completed - Clinical trials for Glycemic Intolerance

Obalon in Children With Severe Obesity

Obalon
Start date: January 2014
Phase: Phase 3
Study type: Interventional

The ongoing global rise in the prevalence of overweight and obesity among all ages and among all ethnic groups, figures into a real epidemic phenomenon. This is accompanied by a higher incidence in serious health risks, already present at an early age, "switching-on" the engine towards obesity-related co-morbid diseases and morbid obesity. Weight loss is the only way to avoid systemic and cardiovascular complications of obesity. Weight loss devices have been recently introduced in bariatric surgery, also in children. They mostly require invasive procedures to be applied. Mini-invasive devices would be needed to obtain weight loss in the pediatric population, since the early age of involved patients. Obalon intragastric balloons, are swallowable devices. They are filled with liquid or air, and have been used to induce weight loss in obese adults. The investigators aimed to perform a pilot study in pediatrics, and monitor weight loss, metabolic and cardiovascular parameters modifications, after up-to-3 Obalon® Gastric Balloons placement.

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: NCT02128802 Active, not recruiting - Renal Failure Clinical Trials

Obesity Surgery and Kidney Transplant for Patients With Obesity and Renal Failure

Start date: April 2014
Phase: N/A
Study type: Interventional

Gastric Bypass followed by renal transplantation is superior to medical management followed by renal transplant for patients with severe obesity and renal failure.

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.