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Bariatric Surgery Candidate clinical trials

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NCT ID: NCT02324946 Completed - Clinical trials for Bariatric Surgery Candidate

Comparison of STOP-BANG and DES-OSA as Predictive Score for Difficult Intubation.

Start date: October 2014
Phase: N/A
Study type: Observational

The DES-OSA Score and the STOP-BANG score were predictive scores for Obstructive Sleep Apnea. This study will compare, among patients scheduled for bariatric surgery, these two scores as predictive scores for a difficult intubation.

NCT ID: NCT02300168 Completed - Clinical trials for Bariatric Surgery Candidate

Neuromuscular Blockade: Outcome and Recovery for Laparoscopic Bariatric Surgery

Start date: September 2014
Phase: N/A
Study type: Observational

The aim of the current observational study is to better assess the relationships between neuromuscular blockade and multiple surgical outcomes in patients undergoing elective laparoscopic bariatric surgery.

NCT ID: NCT02219269 Completed - Cancer Clinical Trials

A Complex Contraception Registry

Start date: June 2014
Phase: N/A
Study type: Observational [Patient Registry]

The investigators will conduct a prospective observational cohort study to investigate factors that influence contraceptive method utilization among women with medical conditions. The investigators will also investigate how women with medical conditions access to contraception and family planning fellowship trained specialist. After the baseline questionnaire, there be a 3 month and 6 month follow up questionnaire to investigate continuation and satisfaction with the contraceptive method. This study is unique because it will allow us to explore doing collaborative family planning research at the multiple UC medical campuses.

NCT ID: NCT02154763 Completed - Clinical trials for Bariatric Surgery Candidate

The Use of Intraperitoneal Ropivacaine in Bariatric Bypass Surgery

INOPAIN
Start date: July 2014
Phase: Phase 3
Study type: Interventional

This is a pilot study in a randomized, controlled, double-blinded format and will evaluate the ability of a local anesthetic, Ropivacaine, to decrease pain after gastric bypass surgery. The drug will be administered into the abdomen during a bariatric bypass surgery. After surgery, patients who received Ropivacaine will be compared to those without Ropivacaine to determine its effect on reducing pain, recovery of lung function, ability to walk, and quality of life during recovery.

NCT ID: NCT02128698 Completed - Clinical trials for Bariatric Surgery Candidate

Physical Activity and Protein Supplementation After Bariatric Surgery (PAPAB)

PAPAB
Start date: March 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine wether regular physical activity in combination with protein supplementation after bariatric surgery can reduce the loss of muscle mass and wether a computer-assisted exercise program is more effective than a usual exercise program regarding frequency of physical activity, fitness and muscular strength.

NCT ID: NCT02121808 Completed - Morbid Obesity Clinical Trials

EPO2-PV: Evaluation of Pre-Oxygenation Conditions in Morbidly Obese Volunteer: Effect of Position and Ventilation Mode

EPO2-PV
Start date: April 2014
Phase: N/A
Study type: Interventional

The risk of complications associated with airway management in obese patients is significant. The results of pre-oxygenation allow a prolonged non-hypoxic apnea time for the clinician. The increase in FRC and non-hypoxic apnea time is correlated. The best condition to accomplish the pre-oxygenation in morbidly obese patient is still undetermined in medical literature. This study is designed to evaluate the effect of different positions combined with different ventilation modes during the pre-oxygenation phase of anesthesia's induction. EPO2: PV will evaluate the effect of different combinations of positions and ventilation modes on pulmonary volumes (mainly functional residual capacity) in a morbidly obese volunteer.

NCT ID: NCT02092376 Completed - Clinical trials for Bariatric Surgery Candidate

The Link Between Obesity And Vitamin D in Bariatric Patients With Omega-loop Bypass Surgery

LOAD
Start date: March 2014
Phase: Phase 4
Study type: Interventional

The aim of the study is to increase vitamin D concentrations or to keep it on high level, respectively, by supplementing with vitamin D3 in a different dose regime, and to improve the overall health status in bariatric patients. In this project, the vitamin D status, the parameters of inflammation, bone turnover, insulin resistance, liver and depression score of bariatric patients are expected to improve, due to supplementation of a loading dose compared to the standard therapy.

NCT ID: NCT02021630 Completed - Obesity Clinical Trials

The Collateral Impact of Bariatric Surgery on Families

Collateral
Start date: December 2012
Phase: N/A
Study type: Observational

This proposal is designed to examine the impact of bariatric surgery on the health of patients and their families. The shared environment of spouses/cohabitating partners suggests that patients' families are exposed to the extensive diet and lifestyle changes required of patients following bariatric surgery.

NCT ID: NCT01475617 Completed - Clinical trials for Bariatric Surgery Candidate

Efficacy of a Novel Multivitamin-Mineral Supplement in Preventing Vitamin Deficiency in Postoperative Bariatric Patients

Start date: November 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Approximately 33% of the US adult population can be classified as obese based on body mass index. This epidemic of obesity has resulted in over 200,000 bariatric surgeries performed every year for the treatment of "clinically severe obesity". Roux-en-Y gastric bypass (RYGB) is the most common bariatric procedure performed in the United States and has both restrictive and malabsorptive components. Despite the success of this procedure in creating long lasting weight loss, vitamin and iron deficiencies are common and can lead to significant morbidity if not appropriately addressed. Despite the American Association of Clinical Endocrinologists, The Obesity Society, and American Society for Metabolic & Bariatric Surgery Medical Guidelines that include vitamin and mineral supplementation recommendations, there has been very little prospective research conducted to assess the efficacy and compliance of these micronutrient interventions. This prospective randomized controlled clinical study will evaluate the efficacy of a novel vitamin/mineral supplement in decreasing micronutrient deficiencies in post operative bariatric patients.

NCT ID: NCT01271062 Completed - Clinical trials for Diabetes Mellitus, Type 2

Restoration of Beta Cell Function and Cardiovascular Parameters in Relation to Adipoinsular and Enteroinsular Axes After Gastric Bypass Surgery

Start date: October 2009
Phase: N/A
Study type: Interventional

Bariatric operations such as the gastric bypass procedure provide a unique in vivo model of improvement of pathological beta cell function. The presented double-centre study aims to comprehensively investigate different aspects of beta cell function in patients with type 2 diabetes (T2DM) with a wide range of disease duration after gastric bypass. In parallel, our project will address the aspects of changes in enteroinsular and adipoinsular axes as well as the early and late changes of other defined parameters after gastric bypass surgery.