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Obesity, Morbid clinical trials

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NCT ID: NCT06018948 Completed - Anesthesia Clinical Trials

Effect of Two Different Doses of Dexmedetomidine Infusion in Morbidly Obese Patients

Start date: September 1, 2019
Phase: Phase 4
Study type: Interventional

Compare the effects of two different doses of dexmedetomidine infusion on oxygenation as a primary outcome and on lung mechanics, quality of recovery and perioperative analgesia as secondary outcomes in morbidly obese patients with restrictive lung disease undergoing abdominal surgery.

NCT ID: NCT05987787 Completed - Clinical trials for Bariatric Surgery Candidate

Suture Reinforcement to Reduce the Leak Rate After Sleeve Gastrectomy

Start date: January 1, 2022
Phase:
Study type: Observational

Staple line reinforcement (SLR) has been suggested as a mean of reducing the risk of sleeve leakage or bleeding. The aim of this study is to analyze if the suture reinforcement can be used to reduce the leakage rate after sleeve gastrectomy.

NCT ID: NCT05854875 Completed - Type 2 Diabetes Clinical Trials

Diabetes Remission After RYGBP and RYGBP With Fundus Resection

Start date: September 22, 2019
Phase: N/A
Study type: Interventional

The goal of this randomized clinical trial is to evaluate glycemic control in patients with morbid obesity and type 2 diabetes after Roux-en-Y gastric bypass (RYGBP) and RYGBP with fundus resection. The main questions to answer are: - Rate of diabetes remission and the role of the gastrointestinal hormones - Whether fundus resection leads to improved glycemic control Patients will randomly undergo typical RYGBP or RYGBP with fundus resection. Gastrointestinal hormones profile [ghrelin, glucagon-like peptide-1 (GLP-1), peptide YY (PYY), glucagon], glucose levels and insulin response will be measured preoperatively, at 6 months and at 12 months, during 120-min OGTT.

NCT ID: NCT05790317 Completed - Diabetes Clinical Trials

Comparison of the Effect of Traditional Method and Eras Protocol in Obesity Surgery

Start date: February 14, 2022
Phase: N/A
Study type: Interventional

This study was conducted to compare the effectiveness of care based on the "Accelerated Recovery After Surgery (ERAS) Protocol" and the traditional method in bariatric surgery and demonstrate the difference the two methods based on evidence.

NCT ID: NCT05746936 Completed - Obesity, Morbid Clinical Trials

Robotic Versus Laparoscopic Roux En-y Gastric Bypass

Start date: January 1, 2020
Phase:
Study type: Observational

This study retrospectively identified 33 consecutive obese patients who underwent either laparoscopic or robotic gastric bypass procedures over a 2-year period.

NCT ID: NCT05608031 Completed - Surgery Clinical Trials

6th Month EWL% After Sleeve Gastrectomy to Get a Better Sleep Quality

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

Obesity, caused by caloric intake over output, has become a global health problem. The relationship between sleep and obesity is widely discussed in the literature. Little is known regarding the compliance of sleep quality and patients' weight loss. This study aimed to review how sleep quality is affected by bariatric surgery, examine whether compliance with sleep quality can be predicted after bariatric surgery, and assess its correlation with excess weight loss.

NCT ID: NCT05603338 Completed - Obesity, Morbid Clinical Trials

Naturally Banded Sleeve Gastrectomy

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

the idea is to use an omental flap or round ligament as a natural band in stead of synesthetic band in bariatric procedures, mainly gastric sleeve

NCT ID: NCT05598840 Completed - Weight Loss Clinical Trials

Efficacy of a Mobile Application to Help in Weight Loss Before Bariatric Surgery

VAMOS
Start date: October 18, 2022
Phase: N/A
Study type: Interventional

The present randomized clinical trial aims to prove the safety and efficacy of an interactive mobile application (Care4Today®) to obtain sufficient weight loss and empower patients with morbid obesity before being submitted to a gastric by-pass.

NCT ID: NCT05591833 Completed - Obesity, Morbid Clinical Trials

Single Anastomosis Sleeve Ileal Bypass Versus Single Anastomosis Sleeve Jejunal Bypass

Start date: July 1, 2022
Phase: N/A
Study type: Interventional

to compare the results of SASI to SAS-J in treatment of morbid obesity

NCT ID: NCT05591105 Completed - Opioid Use Clinical Trials

Morphine Consumption in the Obese Patients

Start date: January 15, 2022
Phase:
Study type: Observational

The goal of this observational study is to evaluate the quality of postoperative analgesia in a group of obese patients schedule to bariatric surgery under TIVA Opiod-free after to receive lidocaine and ketamine perfusion. The main question it aims to answer are: How lidocaine and ketamine perfusion during recovery period does impact over morphine consumption on the following 48 hours after surgery? All participants will receive total intravenous anesthesia and, at the end of the surgery, they will be divided in two groups, group A: placebo and, group B: with postoperative lidocaine and ketamine perfusion. Our hypothesis is ketamine and lidocaine are a good alternative to decrease the use of morphine in obese patients.