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Bariatric Surgery Candidate clinical trials

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NCT ID: NCT05291741 Recruiting - Weight Loss Clinical Trials

Use of Very Low Calorie Diet Preoperatively to Bariatric Surgery

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

To investigate use of Very Low Calorie Diet preoperatively to bariatric surgery can optimize weight loss prior to surgery and increase the patients' satisfaction.

NCT ID: NCT05289219 Recruiting - Clinical trials for Bariatric Surgery Candidate

Effects of Physical Exercise on Sarcopenia After Bariatric Surgery

EXPOBAR
Start date: September 1, 2021
Phase: N/A
Study type: Interventional

The study will include 60 patients awaiting bariatric surgery. They will be randomized into 2 groups, experimental and control. The intervention will take place 1 month after surgery, for a total of 16 weeks. Parameters of body composition, metabolic risk, quality of life, physical activity and sedentary behavior will be determined

NCT ID: NCT05284695 Completed - Clinical trials for Bariatric Surgery Candidate

THE EFFICIENCY OF FASCIAL PLANE BLOCKS IN BARIATRIC SURGERY

Start date: January 1, 2019
Phase:
Study type: Observational

Bariatric surgery effectively produces weight loss and reduces obesity-related comorbidities. Although it is mostly performed with minimally invasive techniques, the patients may still suffer from moderate-to-severe pain immediately after surgery [1]. Opioids remain the first choice for multimodal analgesia in the treatment of postoperative pain. Providing analgesia after bariatric surgery might be challenging due to a high prevalence of obstructive sleep apnea syndrome and the increased sensitivity to respiratory depression triggered by opioid overuse after surgeryThe most common plane block techniques utilized during laparoscopic bariatric surgery are transversus abdominis plane block (TAP), rectus sheath block (RB), the erector spinae plane block (ESPB) and the external oblique intercostal block (EOI). In this study, we have evaluated the auxiliary benefit of these various techniques in reduction of the postoperative in bariatric surgery. patients who had laparoscopic bariatric surgery at VKV American Hospital between January 2019 and December 2021 were reviewed retrospectively.

NCT ID: NCT05273515 Recruiting - Obesity Clinical Trials

Virtual Reality and 3D Reconstruction in Body Image and Bariatrics

Start date: July 13, 2022
Phase: N/A
Study type: Interventional

With obesity on the rise, the number of metabolic procedures performed annually is also increasing. Bariatric surgery has a significant impact on metabolic disease but also results in significant weight loss. Approximately, 30-40% of excess weight is lost within the first year following surgery. One of the motivating factors for surgery for patients is body image dissatisfaction and the stigmatisation of living with obesity, which is linked to low esteem, anxiety and depression. However, studies have indicated that following bariatric surgery, patients continue to experience dissatisfaction with their new body and identity due to unmet expectations. The investigators aim is to start addressing body image issues prior to surgery and provide realistic expectations to patients. This study will be focusing on the feasibility and acceptability of 3D image reconstruction and virtual reality as a method of helping bariatric patients manage their expectations and improve body image satisfaction after surgery. Thereby, leading to better quality of life, improved psychological outcomes and prevention of disordered eating, anxiety and depression. The study will take place at St Mary's Hospital (London) and the West London NHS Trust Bariatric Clinic from March 2022 to September 2022 (7 months). The study aims to recruit 10 participants from the Tier 3 Bariatric Preoperative Group. Once the participant has provided written consent, a photograph of them will be taken using a handheld 3D scanner on a secure password protected device. The images will be processed to produce two reconstructed images, one with 15% less body weight and the second with 25% less body weight. The participants will be divided into groups of 5 and shown their reconstructed images using individual virtual reality headsets. The participants will only have access to their own images. This will be followed up with group peer discussion meetings and questionnaires.

NCT ID: NCT05259111 Recruiting - Clinical trials for Bariatric Surgery Candidate

Home Hospital for Bariatric Sleeve Gastrectomy

Start date: February 23, 2022
Phase: N/A
Study type: Interventional

Providing acute care at home for medicine patients is a well-studied care model. Providing acute care at home immediately following major surgery is less well understood. The investigators seek to demonstrate the noninferiority of care at home versus the hospital for patients undergoing bariatric sleeve gastrectomy.

NCT ID: NCT05258578 Recruiting - Obesity Clinical Trials

Tele-BARICARE to Manage COVID-19-Related Distress

TELE-BARICARE
Start date: October 6, 2022
Phase: N/A
Study type: Interventional

Background: Over 60% of Canadians are overweight or obese and more than half have a history of a mental illness. The COVID-19 pandemic has made it difficult for people living with obesity to manage their weight even after undergoing bariatric surgery. These difficulties in combination with the stress of the pandemic can cause significant declines in mental health and well-being. Psychotherapy ("talk therapy") has been shown to be effective in helping to reduce mental health and disordered eating symptoms in patients managing obesity; however, there is limited data in the context of COVID-19. Objective: This study will examine whether providing a convenient and accessible telephone-based psychotherapy during and potentially after the COVID-19 pandemic will lead to better mental health and disordered eating-related outcomes in patients managing obesity after weight loss surgery. Hypothesis: Relative to the control group, those receiving psychotherapy will have lower mental health distress and eating disorder symptoms. Methods: Participants recruited from 4 weight loss surgery programs across Ontario will be randomly assigned to one of two groups: 1) Control (7 weekly non-structured check-in emails and access to online COVID-19 related mental health resources) or 2) Tele-CBT (a 7-session telephone-based cognitive behavioural therapy [a type of "talk therapy"] intervention focused on developing coping skills and specifically designed for weight loss surgery patients). Participants will complete measures of mental health distress, eating behaviours and a psychological distress scale prior to and immediately following the intervention. Implications: If Tele-CBT is found to improve post-pandemic mental health distress and eating behaviours, it could be routinely offered to patients with other chronic medical conditions as a resource to help manage psychological distress and mental health concerns emerging during and after the COVID-19 pandemic.

NCT ID: NCT05257200 Recruiting - Clinical trials for Bariatric Surgery Candidate

Gut Permeability and Bariatric-metabolic Surgery

Start date: May 1, 2021
Phase:
Study type: Observational

Increased intestinal permeability and dysbiosis have been causally associated with NAFLD and NASH progression. However, to date, there are no systematic studies, on the effect of bariatric-metabolic surgery on intestinal permeability and dysbiosis in the context of NAFLD development.

NCT ID: NCT05235945 Recruiting - Obesity Clinical Trials

The Effect of Exercise in Patients Awaiting Bariatric Surgery

BariPrehab
Start date: June 16, 2023
Phase: N/A
Study type: Interventional

The aim of this project is to understand the impact of a four week preoperative exercise programme on fitness and metabolic rate and weight before surgery and weight after surgery. A single-site randomised trial at UCLH, recruiting patients awaiting bariatric surgery for obesity at UCLH, Whittington Health NHS Trust, or Homerton University Hospital NHS Foundation Trust. The investigators will measure fitness, metabolic rate, body weight/composition and grip strength in all participants, before and after a four-week supervised physical activity intervention. The investigators will also interview participants about their participation in the study in regard to the planning of future studies.

NCT ID: NCT05215886 Enrolling by invitation - Clinical trials for Bariatric Surgery Candidate

Cognitive Impairment, Obesity, and the Effects of Bariatric Surgery

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

Study is designed to screen psychological cognitive baseline and retention/improvement after weight loss surgery.

NCT ID: NCT05208138 Terminated - Clinical trials for Bariatric Surgery Candidate

Feasibility and Safety of Robotic Bariatric Surgery Using the SenhanceTM Surgical System

RoboBar
Start date: January 20, 2022
Phase: Phase 2
Study type: Interventional

Evaluating feasibility and safety of the Senhance Surgical System with digital laparoscopy in bariatric surgery.