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Obesity, Morbid clinical trials

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NCT ID: NCT03391401 Completed - Clinical trials for Bariatric Surgery Candidate

Investigation of Microbiome-based Prognostical Biomarkers in Patients With Morbid Obesity and Bariatric Surgery

Start date: March 1, 2018
Phase:
Study type: Observational

Morbid obesity leads to non-alcoholic fatty liver disease (NAFLD), and not all NAFLD cases benefit from weight loss e.g. after bariatric surgery. Our aim is to find out, which intrahepatic factors and / or biomarkers might be beneficial or can be identified as prognostic factors for remission of NAFLD after weight loss. As other factors such as the microbiome or muscle and fatty tissue also influence the development of obesity and liver diseases, it is planned to examine these parameters before and after bariatric surgery as well. Tissue biopsies will therefore be taken during the surgery, and blood as well as stool samples will be collected and compared for suitable biomarkers before and after the intervention.

NCT ID: NCT03384303 Completed - Morbid Obesity Clinical Trials

Changes in Incretines, Gut Hormones and Bile Acids After Roux-en-Y Gastric Bypass

Start date: October 1, 2015
Phase: N/A
Study type: Interventional

Obesity is an increasing world wide problem. Moreover, the increase in patients who are considered morbidly obese is even higher (Sturm et al, Healt Aff 2004). Conservative approaches such as diets or medication are unsuccessful in the majority of the patients. Additionally, (morbid) obesity leads often to cardiovascular diseases, such as hypertension, dyslipidemia and type 2 diabetes (T2DM). When patients need insulin to regulate their glucose levels, their weight is even more difficult to control. Therefore, bariatric procedures are increasingly performed, with over 8.000 procedures in the Netherlands in 2013. The two most performed types of bariatric surgery in the Netherlands are the Laparoscopic Roux-en-Y Gastric Bypass (LRYGB) and the Laparoscopic Sleeve Gastrectomy (LSG). Within the LRYGB there are different variants available. In a recently initiated randomized controlled trial (RCT) from our centre, a comparison between two variants of RYGB was performed. In this RCT our standard RYGB (s-RYGB:alimentary limb (AL) of 150cm; biliopancreatic limb (BPL) of 75cm) was compared with a RYGB with an long BPL (LBPLRYGB:AL of 75cm and a BPL of 150cm). A LBPLRYGB might improve weight loss and reduction after surgery. The exact mechanism of action is still not fully understood. Stomach volume is decreased and satiety levels often increase, probably due to changes in incretin levels. Passage of foods through the gastrointestinal tract are altered after RYGB. A possible explanation might be found in different levels of incretins (such as GLP-1, PYY and ghrelin) and bile acids (FGF-19 and FGF-21) after bariatric surgery.

NCT ID: NCT03339791 Completed - Surgery Clinical Trials

Sleeve Versus Bypass in Older Patients: a Randomized Controlled Trial

BaSE
Start date: September 23, 2017
Phase: N/A
Study type: Interventional

The aim of the study is to compare two different bariatric procedures performed in patients with 65 years or more: gastric bypass and sleeve gastrectomy. Primary outcomes will be weight loss, control of comorbidities and morbidity of the operation. Secondary outcomes are related to functionality, that will be evaluated with specific tests.

NCT ID: NCT03305432 Completed - Morbid Obesity Clinical Trials

Preoperative PPI in Sleeve Gastrectomy

Start date: January 15, 2018
Phase: Phase 2
Study type: Interventional

he purpose of this study is to study the effect of preoperative PPI in the early outcome of sleeve gastrectomy

NCT ID: NCT03287960 Completed - Clinical trials for Leptin Receptor Deficiency Obesity

Setmelanotide for the Treatment of Leptin Receptor (LEPR) Deficiency Obesity

Start date: January 30, 2018
Phase: Phase 3
Study type: Interventional

To demonstrate statistically significant and clinically meaningful effects of setmelanotide on percent body weight change in participants with LEPR deficiency obesity due to rare bi-allelic or loss-of function mutations at the end of 1 year of treatment.

NCT ID: NCT03286374 Completed - Obesity, Morbid Clinical Trials

Do Change in Life Style Improve Work Ability?

Start date: August 30, 2017
Phase: N/A
Study type: Interventional

The main aim of this Cohort trial is to get more information about how life style changes affect work participation for people with BMI above 30. The information can contribute to improving the quality of occupational rehabilitation programs in the specialized health care services and for others who work with weight loss programs and work related rehabilitation programs.

NCT ID: NCT03283644 Completed - Obesity Clinical Trials

Obesity-related Inflammation in Patients Prior to and After Bariatric Surgery

Start date: June 2015
Phase:
Study type: Observational

This study investigates the chronic long-term health condition of obesity and its effect on neutrophil function and the inflammatory response

NCT ID: NCT03246672 Completed - Obesity, Morbid Clinical Trials

Development of a Weight Maintenance Intervention for Bariatric Surgery Patients

MAINTAIN-B
Start date: January 3, 2018
Phase: N/A
Study type: Interventional

Although bariatric surgery is highly effective for inducing significant weight loss and resolution of comorbidities, weight regain following surgery is a common problem. This pilot study will test the feasibility and acceptability of an intervention designed to help bariatric surgery patients maintain weight loss. Findings from this pilot will provide the foundation for a randomized controlled trial to evaluate the efficacy of the intervention.

NCT ID: NCT03246386 Completed - Morbid Obesity Clinical Trials

Dosing Obese With Noxafil® Under a Trial (DONUT)

DONUT
Start date: November 5, 2017
Phase: Phase 4
Study type: Interventional

Although posaconazole is approved for the prophylaxes and treatment of invasive fungal infections, specific dosing guidelines for posaconazole in (morbidly) obese patients are not specified. There is clear evidence indicating that heavier patients are receiving a sub-optimal dose if the current guidelines are used. Specifically in the setting of augmented prevalence of species with intermediate susceptible to posaconazole, adequate dosing is needed at start of treatment. Therefore it seems prudent to conduct a trial in a cohort of obese patients who receive posaconazole (300mg or 400mg) and define the pharmacokinetics. These will then be compared to the pharmacokinetics in a normal-weight group receiving 300mg posaconazole.

NCT ID: NCT03240367 Completed - Obesity, Morbid Clinical Trials

Comparison of Stapler Line Bleeding Control Techniquessurgery

Start date: December 4, 2016
Phase: N/A
Study type: Interventional

Introduction RYGB surgeon; Have become increasingly morbid obesity treatment methods with improvements in minimally invasive surgery. Ensuring patient comfort and early return to life are the criteria that should be given priority in this treatment method.The purpose of this study; Emphasizing that the cautery technique of the stapler line bleeding control methods is as successful as the other methods.