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Obesity, Morbid clinical trials

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NCT ID: NCT03434522 Active, not recruiting - Obesity, Morbid Clinical Trials

vBloc Now - Registry

Start date: December 27, 2017
Phase:
Study type: Observational

This is a prospective, observational, case series registry which will collect information pertaining to experiences and health economics in individuals implanted with vBloc Therapy who are conjunctively using a weight management program. Subjects will be followed for 12 months after implant.

NCT ID: NCT03429205 Terminated - Morbid Obesity Clinical Trials

The Efficacy of External Warming During Laparoscopic Bariatric Surgery

Start date: March 15, 2018
Phase: N/A
Study type: Interventional

External warming is routinely used in general surgery to offset the deleterious effects of hypothermia. It entails deployment of a disposable, external heating blanket attached to a regulated hot-air pump. The need for external warming in the morbidly obese population undergoing short laparoscopic procedures is unclear. If proven to be unnecessary, time and momentary costs could be lowered. The study will compare core-temperature dynamics during laparoscopic bariatric procedures anticipated to last <2h. The study group will be left without a warming blanket while the control group will receive routine external warming. Post-anesthesia care unit (PACU) arrival temperature will also be recorded.

NCT ID: NCT03428386 Recruiting - Morbid Obesity Clinical Trials

Single-Anastomosis Plication Ileal Bypass for Morbid Obesity

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

The present study aims to explore the impact of combining laparoscopic greater curvature plication with a single gastro-ileal anastomosis in the same manner of single anastomosis sleeve ileal bypass on weight loss and postoperative complications. The objective of this combined procedure is to reduce the high intraluminal pressure that results after laparoscopic greater curvature plication owing to reduced intraluminal space which can lead to suture line leakage, vomiting, and gastroesophageal reflux disease. Another objective is to add a malabsorptive element to the restrictive effect of laparoscopic greater curvature plication and to induce early satiety in patients by distention of the distal bowel with nutrients immediately after meals, similar to the way that single anastomosis sleeve ileal bypass works.

NCT ID: NCT03419273 Completed - Clinical trials for Bariatric Surgery Candidate

Adipose Tissue Inflammation in Individuals Undergoing Bariatric Surgery

Start date: July 1, 2017
Phase:
Study type: Observational

A growing body of work done over the past few decades has established that adipose tissue as an active endocrine organ which secretes a wide range of metabolic and immunological factors collectively called "adipokines (1)." Importantly, these secreted factors enter into the circulation and have paracrine and autocrine actions, which profoundly impact systemic metabolism (e.g., insulin sensitivity). Additionally, in animals, loss of ovarian hormone production via ovariectomy (similar to menopause in humans) leads to increases in both in adipose tissue mass and in adipose tissue inflammation (2) making this tissue less healthy than that from premenopausal animals. To date, no studies have investigated the effect of menopause on abdominal fat in overweight individuals. Knowing if adipose tissue-specific changes occur with menopause may potentially lead to recommendations or therapeutics to improve women's health post menopause.

NCT ID: NCT03419104 Recruiting - Morbid Obesity Clinical Trials

Preoperative Exercise Test and Postoperative Intensive Care Unit Need in Bariatric Surgery

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The aim of our study is to evaluate the efficacy of "60 meters 60 seconds exercise test" (a test designed by the study group) done preoperatively as a predictor test for postoperative intensive care unit need and extubation success in patients undergoing bariatric surgery.

NCT ID: NCT03411772 Completed - Morbid Obesity Clinical Trials

Trial on TAP Block After Bariatric Surgery

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

Patients undergoing bariatric surgery will be divided randomly into two groups: the first will have TAP block upon completion of surgery and the second groups will not have TAP block.

NCT ID: NCT03410849 Completed - Morbid Obesity Clinical Trials

Long-term Adverse Effects After Bariatric Surgery on Oesophagus Epithelium

FUB-B
Start date: February 1, 2018
Phase: N/A
Study type: Interventional

The goal of this trial is to examine long-term effects of laparoscopic gastric bypass (LRYGB) and sleeve gastrectomy (LSG) on oesophageal symptoms and disease, including the presence of Barrett oesophagus ≥ 5 years post-surgery.

NCT ID: NCT03410459 Completed - Morbid Obesity Clinical Trials

Long-term Adverse Effects After Bariatric Surgery on Bone Density

FUB-A
Start date: February 2, 2018
Phase: N/A
Study type: Interventional

The goal of this trial is to examine long-term effects of laparoscopic gastric bypass (LRYGB) and sleeve gastrectomy (LSG) on bone mineral density, fracture risk, and body composition ≥ 5 years post-surgery.

NCT ID: NCT03405311 Terminated - Pain Clinical Trials

3D Ultrasound-guided Labor Epidural Analgesia in the Morbid Obese Parturient

Start date: February 20, 2018
Phase: N/A
Study type: Interventional

This study will be a randomized control study, with the objective to evaluate epidural analgesia success rates between the two methods (Blind Approach versus Accuro Device).

NCT ID: NCT03391817 Recruiting - Obesity, Morbid Clinical Trials

FAECAL MICROBIOTA TRANSPLANTATION IN OBESITY

Start date: January 19, 2018
Phase: N/A
Study type: Interventional

40 patients meeting the criteria for obesity surgery are enrolled. Fecal microbiota transplantation (FMT) will be administered in gastroscopy 6 months before obesity surgery. 20 of the patients will receive a fecal transplant of a thin donor and 20 will receive placebo - a transplant made of their on feces. Changes in weight, laboratory values, general well being and stool microbiota will be measured up to one year after the surgery; one and a half years after FMT. The hypothesis is that FMT and the change in gut microbiota will help to reduce and maintain lower weight.