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Bariatric Surgery Candidate clinical trials

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NCT ID: NCT03833011 Completed - Pain Clinical Trials

Postoperative Osteopathic Manipulative Treatment in Bariatric Surgery

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

Context Pain control is one of the most challenging problems encountered in postoperative period in bariatric patients. Currently there are no published studies evaluating Osteopathic Manipulative Treatment in bariatric surgery patients. Objective The primary objective of this study is to determine whether Osteopathic Manipulative Treatment (OMT) can decrease pain score in bariatric patients. The secondary objective is whether OMT can improve patient satisfaction with overall treatment. Design: A prospective randomized group controlled study. Setting: A 293-bed non-for-profit teaching community hospital. Methods Thirty-six patients scheduled for bariatric surgery as per ASMBS criteria were eligible for study from January 2017 through August 2018 at Flushing Hospital Medical Center, New York. Twelve patients were excluded. Twenty-four patients were included into study and randomized to receive OMT(n=12) vs Control (n=12) intervention. In Control group, patients received standard pain control protocol with morphine patient controlled analgesia pump (PCA) In OMT group, patients received standard postoperative pain protocol and OMT on postoperative day one. Three techniques were used (Sub-occipital Release, Thoracic Outlet Release, and Rib Raising). All patients received survey to complete prior to discharge measuring pain score (1-10), patient satisfaction score 1-4 (poor, fair, good, excellent) and data was analyzed.

NCT ID: NCT03832439 Completed - Clinical trials for Bariatric Surgery Candidate

Probiotic Supplementation on Weight Loss

Start date: January 17, 2019
Phase: N/A
Study type: Interventional

The investigators are trying to better understand how bariatric surgery leads to weight loss, and the role of bacteria that live in the gut in making this happen.

NCT ID: NCT03828513 Active, not recruiting - Clinical trials for Bariatric Surgery Candidate

Can the Effects of High Flow Nasal Cannula Oxygenation on Postoperative Atelectasis be Evaluated With Lung Ultrasound

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

Evaluate the effects of high-flow nasal oxygen therapy on atelectasis in the perioperative period by lung ultrasound (LUS) in bariatric surgery patients.

NCT ID: NCT03817541 Recruiting - Clinical trials for Bariatric Surgery Candidate

Expiratory and Plasma Propofol Concentration in Gastrological Surgery Patients

Start date: November 14, 2018
Phase: N/A
Study type: Interventional

Determination of accuracy With Edmond (reg) expiratory propofol measurement Device, compared With concommitant plasma samples of propofol

NCT ID: NCT03809182 Completed - Insulin Resistance Clinical Trials

Effect of Dexmedetomidine on Postoperative Glucose and Insulin Levels.

Start date: September 27, 2012
Phase: Phase 4
Study type: Interventional

This study investigated the effect of dexmedetomidine in obese patients undergoing bariatric surgery.

NCT ID: NCT03798522 Completed - Morbid Obesity Clinical Trials

Erector Spinae Plane Block Versus Opioid Based General Anesthesia During Laparoscopic Bariatric Surgery

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

bilateral continuous erector spinae plane blockade may represent a valuable alternatives to thoracіc epidurals analgaesіa in treatment of thoracic neuropathic pain. There were 3 cases reported in 2017 suggested that the erector spinae plane block provides visceral abdominal analgesia in bariatric surgery and at end of the report they recommended further clinical investigation. The investigators hypothesіzed that performing the erector spinae plane (ESP) block at T7 would provide effective abdominal analgaesіa іn patients undergone laparoscopic bariatric surgery. The investigators aimed to compare the analgesic effect of erector spinae plane block and opioid based general anesthesia for laparoscopic bariatric surgeries.

NCT ID: NCT03792412 Recruiting - Malnutrition Clinical Trials

BagEL - Bariatric Patients in Primary Care: Post-operative Nutrition and Lifestyle Management

Start date: May 22, 2018
Phase: N/A
Study type: Interventional

There is a growing number of patients undergoing bariatric surgery requiring lifelong follow-up. BagEL (Bariatric Patients in Primary Care: Post-operative Nutrition and Lifestyle Management) is a survey to evaluate a newly developed structured disease management program including nutrition and lifestyle management in primary care.

NCT ID: NCT03783052 Completed - Obesity Clinical Trials

Gastrointestinal Physiological Conditions in Obesity and After Bariatric Surgery

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

Over the years, obesity has become a major public health concern. The increasing rates of obesity are associated with an enhanced demand for weight-loss with bariatric surgery as a treatment option. Bariatric surgery procedures alter the anatomical structure of the gastrointestinal tract, which contributes to the postoperative weight loss. However, it is not sure how obesity and the anatomical alterations of bariatric surgery affect the gastrointestinal physiology including gastrointestinal pH, gastric emptying, intestinal transit time and concentration of enzymes.

NCT ID: NCT03758898 Completed - Clinical trials for Bariatric Surgery Candidate

The Effect of Chest Physiotherapy After Bariatric Surgery

Start date: May 5, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the effect of chest physiotherapy applied to patients undergoing bariatric surgery on pulmonary functions, dyspnea levels, functional capacity and quality of life.

NCT ID: NCT03747406 Completed - Clinical trials for Bariatric Surgery Candidate

Erector Spinae Block and Transverse Abdominis Plane Block for Sleeve Gasterectomy

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

assess the efficacy of ultrasound guided erector spinae block to decrease the requirement for analgesics after laparoscopic sleeve gastrectomy and to decrease postoperative pain scores and opioid consumption compared to subcostal transverses abdominis block.