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Obesity, Morbid clinical trials

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NCT ID: NCT02929212 Completed - Morbid Obesity Clinical Trials

Effect of Number of Meals on Metabolism After Weight Loss Surgery

LAF 28
Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of meal size and texture on the levels of incretin hormone, GLP-1, after Gastric Bypass Surgery (GBP). Patterns of food intake change after bariatric surgery and patients often eat multiple small low-calorie meals, a pattern that may affect blood glucose as well as incretin levels. Whether the release of GLP-1 after an oral challenge or a single liquid meal has any physiological relevance in 'real life' setting of multiple small meals diet is unclear.

NCT ID: NCT02904291 Recruiting - Obesity, Morbid Clinical Trials

Bariatric Surgery and Pharmacokinetics of Amlodipine

Start date: November 2016
Phase:
Study type: Observational

Changes to gastric pH, gastric emptying time, gastrointestinal transit-time or the pre-systemic metabolizing effect of enzymes secreted in the mucosa may all alter the pharmacokinetics of medicines. These factors are potentially influenced by bariatric surgery. Little is so far known about how gastric bypass and sleeve gastrectomy impacts the biological availability of medication. In this study we investigate the pharmacokinetic effects of bariatric surgery on amlodipine.

NCT ID: NCT02901613 Recruiting - Morbid Obesity Clinical Trials

Prophylactic Post-Cesarean Incisional Negative-pressure Wound Therapy in Morbidly Obese Patients

Start date: August 2016
Phase: N/A
Study type: Interventional

To evaluate the effectiveness of negative-pressure wound therapy in decreasing wound complications in morbidly obese patients (BMI greater than of equal to 40) at Albany Medical Center Hospital. Retrospective data will be collected regarding morbidly obese patients who have undergone cesarean section and patients will be recruited to have the intervention (negative-pressure wound therapy) applied and outcomes will be evaluated.

NCT ID: NCT02882685 Active, not recruiting - Morbid Obesity Clinical Trials

Comparison of Mini Gastric Bypass and Roux-en-Y Gastric Bypass

RYSA
Start date: July 2016
Phase: N/A
Study type: Interventional

This study compares Roux-en-Y gastric bypass with single anastomosis gastric bypass in a randomized prospective setting. This study also adresses the issue of bile reflux after MGB.

NCT ID: NCT02878525 Completed - Morbid Obesity Clinical Trials

Laparoscopic Internal Gastric Banding, New Simple and Costless Weight Loss Procedure

LIGB
Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to study the effectiveness of laparoscopic internal gastric banding as a treatment for morbid obesity in comparison to laparoscopic sleeve gastrectomy

NCT ID: NCT02876484 Completed - Severe Obesity Clinical Trials

Effects of Bile Acids and Bile Acid Sequestrants on GLP-1 Secretion After Roux-en-Y Gastric Bypass

Start date: June 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the effects of bile acid and bile acids sequestrants on GLP-1 Secretion, during a meal, in patients after Roux-en-Y gastric bypass.

NCT ID: NCT02870530 Completed - Morbid Obesity Clinical Trials

Single Anastomosis Sleeve Jejunal (SAS-J) Bypass

Start date: November 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of single anastomoses sleeve jejunal bypass as a treatment for morbid obesity

NCT ID: NCT02859597 Completed - Morbid Obesity Clinical Trials

Use of High Flow Nasal Cannula During Sedation of Morbidly Obese Patients in the Endoscopy Suite

Start date: December 28, 2016
Phase: N/A
Study type: Interventional

This study evaluates the ability of high flow nasal cannula versus nasal cannula to oxygenate morbidly obese patients undergoing moderate to deep sedation for gastrointestinal procedures.

NCT ID: NCT02823561 Completed - Severe Obesity Clinical Trials

Garcinia Mangostana Extracts in the Management of Weight Loss

Start date: November 2015
Phase: Phase 4
Study type: Interventional

Obesity is one of the greatest public health challenges of the 21st century. Its prevalence has tripled in many countries of the European Region since the 1980s, and the numbers of those affected continue to rise at an alarming rate. In addition to causing various physical disabilities and psychological problems, excess weight drastically increases a person's risk of developing a number of noncommunicable diseases including cardiovascular disease, cancer and diabetes, in association or not to metabolic syndrome. The risk of developing more than one of these diseases (co-morbidity) also increases with increasing body weight. Every year a growing number of patient tend to suffer of more severe obesity and difficulty in losing weight even with a restricted diet and exercise. Garcinia mangostana (Sphaeranthus indicus extract) has known for its antioxidant properties; new evidence point out some promising effects in the prevention of lipogenesis and the promotion of lipolysis . Currently in the scientific literature there is only one paper, by Stern et al., showing the association of Garcinia mangostana assumption in low-calorie diet. This work has demonstrated a significant reduction in weight loss , compared to the placebo group,due to the use of Garcinia mangostana. Aim of the present study is the evaluation of safety and efficacy of weight loss in severe obese patients. Also cardiometabolic parameters and flogosys serum indicators will be evaluated before and after 6 month therapy of low calory diet alone or in association with Garcinia mangostana extract.

NCT ID: NCT02811900 Recruiting - Morbid Obesity Clinical Trials

An Evaluation of the Outcomes of Bariatric Surgery - a Cohort Study

ChirBar
Start date: January 1996
Phase: N/A
Study type: Observational [Patient Registry]

A prospective bariatric database was carried out in the Department of Digestive and Endocrine Surgery at the University Hospital of Strasbourg, France, starting in January 1996. All potential candidates for obesity surgery were prospectively registered in the database. Patients were informed by the bariatric surgeon of the prospective database, and of the possibility of utilizing personal data for research purpose after anonymization. A case-control study was performed, to compare the quality of life (QoL) of patients treated for internal hernia (IH group) with the QoL of patients with an uncomplicated course after Roux en Y gastric bypass (Uncomplicated RYGB group).