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Obesity, Morbid clinical trials

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NCT ID: NCT03593798 Completed - Physical Capacity Clinical Trials

Lifestyle Intervention and Physical Capacity in Patients With Morbid Obesity

LEICO
Start date: November 1, 2013
Phase:
Study type: Observational

Lifestyle intervention and physical capacity in patients with morbid Obesity (LEICO)

NCT ID: NCT03590951 Completed - Pregnancy Related Clinical Trials

Anesthetic and Obstetric Outcomes in Morbidly Obese Pregnancy and Cesarean Delivery

Start date: May 3, 2017
Phase:
Study type: Observational

Given that morbid obesity has been strongly associated with obstetric, neonatal and anesthetic complications, and that scarce reports have evaluated anesthetic and obstetric outcomes after cesarean delivery in morbidly obese patients; This study retrospectively analyzed anesthetic, obstetric and neonatal outcomes in morbidly obese pregnant patients who underwent cesarean delivery at Augusta University Medical Center, during a 2-year period (2015-2016).

NCT ID: NCT03578211 Completed - Obesity, Morbid Clinical Trials

Impact of Decision Aids on Bariatric Surgery Choice

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

Sleeve gastrectomy, Roux-en-Y gastric bypass, laparoscopic gastric banding, and bioenteric intragastric balloon insertion are common types of bariatric surgeries. These treatment strategies have diverted outcomes in body weight loss, metabolic diseases control, surgical complications, and life quality improvement. Thus, shared decision making (SDM) is necessary to aid patients to choose an appropriate treatment that suits thier needs. Investigators have developed a decision aids (DAs) and plan to conduct a randomized controlled trial (RCT) to evaluate its impact on obese patients. The measurements include a battery of interview-based questionnaires and evaluations of decision regret and knowledge improvement. Investigators expect the DAs would benefit the intervention group in the aspects of knowledge, communication and anxiety status during and after their treatment sessions.

NCT ID: NCT03563287 Completed - Clinical trials for Bariatric Surgery Candidate

Effects of LRYGB on Pharmacokinetics of Nine CYP Probe Drugs

Start date: January 27, 2012
Phase: N/A
Study type: Interventional

Due to anatomical and physiological changes caused by the Roux-en-Y gastric bypass (RYGB) bariatric surgery, drug bioavailability after the surgery can be altered. Therefore, post-operative dose adjustment in these patients can be required. The aim of the study was to investigate the effects of laparoscopic Roux-en-Y gastric bypass (LRYGB) surgery on drug pharmacokinetics and cytochrome P450 (CYP) mediated metabolism using a cocktail of nine CYP probe drugs. The cocktail covers nine main CYP enzymes: melatonin (CYP1A2), nicotine (CYP2A6), bupropion (CYP2B6), repaglinide (CYP2C8), losartan (CYP2C9), omeprazole (CYP2C19/CYP3A4), dextromethorphan (CYP2D6), chlorzoxazone (CYP2E1), midazolam (CYP3A4). The changes in pharmacokinetic parameters of the drugs as well as modulation of the activity of CYPs are evaluated before and one year after LRYGB. In the study, the patients administering drug cocktail before surgery and 1 year after LRYGB are served as their own controls.

NCT ID: NCT03556306 Completed - Obesity, Morbid Clinical Trials

Intraoperative Findings and Complications in Bariatric Surgery

Start date: January 1, 2013
Phase:
Study type: Observational

Retrospective study with patients submitted to bariatric surgery between 2013 and 2016 at a single Institution. The objective was to analyze the incidence and causes of unexpected intraoperative findings and complications, change in surgical plan, extra surgeries and procedure interruption. All operative information was collected prospectively and aimed to describe any of the previous situations. Secondarily, a morbidity analysis was performed, correlating intraoperative complications with postoperative complications and length of stay.

NCT ID: NCT03555864 Completed - Obesity, Morbid Clinical Trials

Intravenous Access Using Infrared Laser

AccuV
Start date: November 6, 2017
Phase:
Study type: Observational

Peripheral venous access is a prerequisite for anesthesiological for surgical patients.It is often difficult to establish and potentially painful in obese patients (Body mass Index > 35). AV300 uses near infrared laser light to improve visibility of peripheral veins and could help cannulating them. The aim of this study was to examine if use of Accuvein(®) AV300 vein viewer could facilitate venous cannulation in obese patients (surgical and obstetric).

NCT ID: NCT03553849 Completed - Morbid Obesity Clinical Trials

Utilization of Very Low Calorie Diet in Obese General Surgery Patients

Start date: September 24, 2018
Phase: N/A
Study type: Interventional

The investigators are studying the use of a two-week very low calorie diet (VLCD) in obese general surgery patients in a randomized single-blinded trial. The investigators hypothesize that the VLCD will positively impact the perceived surgical difficulty, operative time, hospital length of stay and 30-day complications. Additionally, the investigators anticipate reduced perioperative blood glucose levels and a reduced need for perioperative insulin administration.

NCT ID: NCT03532646 Completed - Clinical trials for Bariatric Surgery Candidate

Endoscopic Complications After Gastric Bypass

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

Endoscopic complications such as gastro-esophageal reflux disease, ulcera, gastritis, bile reflux, anastomotic stricture and so on are described after gastric bypass surgery. The incidence of these complications after RYGB versus MGB/OAGB are getting observed.

NCT ID: NCT03529461 Completed - Hypoxia Clinical Trials

Use of Non-Invasive Positive Pressure Ventilation in Patients With Severe Obesity Undergoing Upper Endoscopy Procedures

Start date: April 25, 2017
Phase: N/A
Study type: Interventional

The study evaluated the effect of non-invasive positive pressure ventilation (NIPPV) to decrease the incidence of desaturation events in patients with severe obesity undergoing upper endoscopy.

NCT ID: NCT03526263 Completed - Obesity Clinical Trials

Endoscopic Gastric Mucosal Devitalization (GMD) as a Primary Obesity Therapy

GMD
Start date: June 7, 2018
Phase: N/A
Study type: Interventional

Rapid metabolic improvements seen with sleeve gastrectomy are likely a result of changes in gastric origin. The gastric mucosa is an endocrine organ that regulates satiation pathways and is a complex regulator of food intake as well as lipid and glucose metabolism. This study aims to assess the efficacy and safety of endoscopic selective gastric mucosal devitalization (GMD) for the management of obesity and its related comorbidities.