Clinical Trials Logo

Bariatric Surgery Candidate clinical trials

View clinical trials related to Bariatric Surgery Candidate.

Filter by:

NCT ID: NCT04883268 Completed - Clinical trials for Bariatric Surgery Candidate

Focusing on Body Functionality After Bariatric Surgery

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

This study investigated whether focusing on one's body functionality (i.e., everything the body can do, rather than how it looks) would lead to improvements in body image, self-esteem, and self-kindness among women who have undergone bariatric surgery.

NCT ID: NCT04880902 Completed - Clinical trials for Bariatric Surgery Candidate

Volumetric Pouch Study After Laparoscopic Sleeve Gastrectomy

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

This study aimed to evaluate Laparoscopic Sleeve Gastrectomy in the treatment of morbidly obese patients pre and post-operatively after 3 months, 6 months, and 1-year follow-up and assess the volumetric changes of the gastric reservoir 1 year after LSG using multi-slice computer tomography.

NCT ID: NCT04879667 Completed - Clinical trials for Bariatric Surgery Candidate

Endoscopic Management Of Refractory Gastro-cutaneous Fistula After Laparoscopic Sleeve Gastrectomy l

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study included patients who were admitted to investigators' center to do laparoscopic sleeve gastrectomy and complicated by gastro-cutaneous fistula . Cases were collected in the period from December 2019 to march 2021. The study was approved by the research and Ethics committee of investigators' University .a written informed consent was obtained from all participating patients after explaining to them all the study procedures with its benefits and hazards. the work has been carried out in accordance with the code of ethics of the world medical association ( Declaration of Helsinki ) for studies involving humans .the sample size was calculated using open Epi program using the following data ; confidence interval 95% , power of test 80% , ratio of unexposed/exposed 1, percent of patients with successful management of refractory gastro-cutaneous fistula by surgical intervention 50% and those with successful management by endoscopy 99% , odds ratio 99%, and risk ratio 2 , so the calculated sample size equal 30 patients divided into two equal groups. Group (1) included 15 patients managed by surgical intervention , group (2) included 15 patients managed by endoscopic intervention.

NCT ID: NCT04878640 Completed - Clinical trials for Bariatric Surgery Candidate

Sleeve Gastrectomy and Cholecystectomy Are Safe in Obese Patients With Asymptomatic Cholelithiasis

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

Introduction: Obesity is an increasingly serious public health problem on a global level. Gallstones may become symptomatic after sleeve gastrectomy surgery. There is a debate regarding concomitant cholecystectomy during bariatric surgery. Aim of the study: This study analyzed outcomes of laparoscopic sleeve gastrectomy (LSG) with and without concomitant laparoscopic cholecystectomy in morbid obese patients with gall bladder stones. Patients and methods: We conducted randomized clinical study on 222 patients. These patients were categorized into two equal groups (111 in each group) .Group A: underwent SG and concomitant laparoscopic cholecystectomy in morbid obese patient with evidence of gall bladder stone, Group B: SG only without concomitant LC inspite of evidence of gall bladder stone. This study was performed at single institution from January 1, 2016 to January 1, 2019.

NCT ID: NCT04868279 Recruiting - Clinical trials for Bariatric Surgery Candidate

Weight Regain After Bariatric Surgery and Web-Based Interactive Nurse Support Program: Mixed Methods Research

Start date: April 23, 2021
Phase: N/A
Study type: Interventional

This study was planned to determine the effect of the web-based interactive nurse support program developed in line with the Health Promotion Model on healthy living behaviors and self-efficacy in individuals who gain weight after bariatric surgery. Mixed method is a research. The exploratory sequential design, one of the mixed research methods, will be used. The research will continue with the quantitative part starting with the qualitative part. The quantitative part of the research is a randomized controlled experimental study.

NCT ID: NCT04852198 Recruiting - Obesity Clinical Trials

Comparing 150cm OAGB With 150cm Biliopancreatic Limb RYGB. A Non-inferiority Trial

Roux-en-WHY?
Start date: December 13, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and efficiency of OAGB compared to RYGB

NCT ID: NCT04851470 Active, not recruiting - Obesity Clinical Trials

Periodontal Assessment of a Bariatric Care Population

Bariatric
Start date: January 31, 2014
Phase:
Study type: Observational

Our primary aim is to investigate the prevalence and severity of Periodonotal Disease (PD) in a population of obese patients. Our secondary objectives are to: Investigate inflammatory biomarkers that have been associated with PD in the saliva of obese patients. Investigate the association of FTO gene (Obesity) polymorphisms with the prevalence of PD in this population. Investigate and describe the subgingival microbial flora in obese patients with PD from subgingival dental plaque samples as well as the salivary samples.

NCT ID: NCT04847843 Recruiting - Obesity Clinical Trials

Eating Mindfully to Prevent Weight Regain

EMPWR
Start date: June 16, 2021
Phase: N/A
Study type: Interventional

The overall objective of this study is to evaluate the efficacy of a mindfulness-based intervention to prevent weight regain in weight-reduced adults.

NCT ID: NCT04847037 Active, not recruiting - Clinical trials for Bariatric Surgery Candidate

Place of Connected Tools in Bariatric Patients Follow-up.

Start date: March 5, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to assess the safety (in terms of post-operative complications) of the use of connected devices for the monitoring of patients operated on by longitudinal laparoscopic gastrectomy (LSG) and discharged 24 hours after surgery according to the protocol Enhanced Recovery After Surgery (ERAS).

NCT ID: NCT04836819 Completed - Pain Clinical Trials

Analgesia Management in Bariatric Surgery

Start date: April 8, 2021
Phase: N/A
Study type: Interventional

Following laparoscopic bariatric surgery, multimodal analgesia is recommended to avoid the adverse effects of opioids by reducing their use. Although lidocaine, ketamine, and dexmedetomidine have been used as adjuvant analgesics, no studies have evaluated the superiority of their intra- and postoperative infusions as components of multimodal analgesia in bariatric surgery. The present study is aimed to compare lidocaine, dexmedetomidine, and ketamine in multimodal analgesia management following Sleeve Gastrectomy Surgery. Postoperative pain scores, the requirement for additional postoperative analgesia, retching, nausea and vomiting, time to mobilization, and hospital length of stay will be evaluated.