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Obesity, Morbid clinical trials

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NCT ID: NCT01790464 Completed - Morbid Obesity Clinical Trials

Glossopharyngeal Nerve Block for Awake Intubation

Start date: April 2012
Phase: N/A
Study type: Interventional

Endotracheal intubation of the morbidly obese is often performed awake. This is performed after topical anesthesia of the patient's pharynx and larynx. There are many techniques used to perform topical anesthesia of the patient's airway, which include aerosolization of local anesthesia, topical application of local anesthesia, and nerve blockade using needles and local anesthesia. Reasons for failure of any awake tracheal intubation technique is excess gagging. The most effective method to adequately anesthetize the airway to decrease the amount of gagging is unknown. The investigators wish to assess if the instillation of local anesthesia soaked gauze next to the peritonsillar pillars will decrease the number of gagging episodes during awake video laryngoscopy assisted tracheal intubation of the morbidly obese.

NCT ID: NCT01784510 Completed - Morbid Obesity Clinical Trials

Two or Six cm From Pylorus at Laparoscopic Sleeve Gastrectomy

Start date: n/a
Phase: N/A
Study type: Interventional

Randomized controlled trial comparing between two technique of laparoscopic sleeve gastrectomy for treatment of morbid obesity. In the first technique the investigators started dissection of gastrocolic ligament 6 cm from pylorus and in the second one the distance was only 2 cm. The main primary outcome measure was weight loss.

NCT ID: NCT01778738 Completed - Type 2 Diabetes Clinical Trials

Type 2 Diabetes After Sleeve Gastrectomy and Roux-en-Y Gastric Bypass: A Randomised Single Centre Study

OSEBERG
Start date: January 2013
Phase: N/A
Study type: Interventional

Glycaemia, insulin secretion and action in morbidly obes subjects with type 2 diabetes after sleeve gastrectomy ond Roux-en-Y gastric bypass: A randomised single centre study.

NCT ID: NCT01774682 Completed - Morbid Obesity Clinical Trials

Kinematics of Obese Patients Perambulation

MARCHOBESE
Start date: January 2013
Phase: Phase 3
Study type: Interventional

The aim of this study is to evaluate the consequences of sleeve gastrectomy on functional parameters of patients perambulation.

NCT ID: NCT01764555 Completed - Morbid Obesity Clinical Trials

Pharmacokinetics of Acetaminophen in Morbidly Obese Patients

APAP
Start date: December 2012
Phase: Phase 4
Study type: Interventional

This study will investigate the pharmacokinetics of acetaminophen in morbidly obese patients versus normal weight patients. Specifically the different metabolic pathways of acetaminophen in morbidly obese adults will be investigated; glucuronidation, sulphation and CYP2E1 (cytochrome P450 2E1) oxidation

NCT ID: NCT01760512 Completed - Morbid Obesity Clinical Trials

Clinical and Health Economic Impact of Robot-assisted Surgery vs Conventional Laparoscopy : the Case of Gastric Bypass

Start date: November 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to gather clinical and economic evidence on the use of robotics for bariatric surgery (gastric bypass). This monocentric, randomized, single blind, controlled study will evaluate post-operative pain, quality of life and appetite, post-operative complication incidence. It will also provide information on direct and indirect costs of surgery.

NCT ID: NCT01759667 Completed - Obesity Clinical Trials

DIT After RYGB - A Prospective Study

DIT RYGB
Start date: August 2012
Phase: N/A
Study type: Interventional

Bariatric surgery is the only satisfactory treatment for loss and weight maintenance in obese patients. This loss is a result of several factors that go beyond the simple anatomical abnormality of the gastrointestinal tract and may be the product of post-op energy expenditure changes. The respiratory quotient (RQ) and diet-induced thermogenesis (DIT) are important components of energy expenditure and possible changes in them can perform an important role in weight loss after Roux-en-Y Gastric Bypass (RYGB). Previously, we conducted a cross-sectional study where we measured the RQ and DIT in pre and post-op RYGB patients, which was published in the Surgery of Obesity and Related Diseases (SOARD) journal. The objective of this study is to perform a prospective analysis of these same variables (RQ and DIT), evaluating them in the same patients, when pre and postoperatively.

NCT ID: NCT01754194 Completed - Morbid Obesity Clinical Trials

Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-en-Y Gastric Bypass Surgery

OPTIMIZE
Start date: April 2012
Phase: N/A
Study type: Observational

Study objectives: 1. generate local clinical, health-related quality-of-life and health economic data to evaluate the benefits of two types of minimally invasive weight-loss surgery 2. support multi-disciplinary bariatric sites in Germany by providing structured procedure guidelines and training, therefore facilitating procedural adoption, increasing safety and shortening the learning curve for weight-loss surgery.

NCT ID: NCT01748682 Completed - Morbid Obesity Clinical Trials

Very Low Calorie Liquid Diet for Pre op Patients

Start date: January 2011
Phase: N/A
Study type: Interventional

Despite the relative consensus on the benefits of pre-surgical weight loss, i.e., the reduction of comorbidities associated with surgical act, such as decreased visceral fat, liver volume, hemorrhage perioperative and surgical time, the characteristics of the diet to be employed in this period need to be defined more clearly. As there is no description of comparative studies on diet of normal consistency, using solids and liquids, there are doubts as to the real need for consistency liquid diet in preoperative bariatric surgery. The lack of robust evidence has made nutrition professionals adopt different procedures. There is still a belief that these patients are unable to lose weight in the preoperative period, the ongoing history of previous attempts without success.

NCT ID: NCT01748513 Completed - Clinical trials for Anomaly; Venous Return

Volume-challenge in Morbid Obesity

Start date: March 2011
Phase: N/A
Study type: Observational

Preoperative venous return stability and euvolemia is essential in management of morbidly obese patients. Fluid therapy regimes for patients with high BMI, especially with focus on preoperative management, are rare and not in consensus.The aim of this study was to evaluate preoperative effects of a standardized, ideal body weight (IBW) based volume-challenge on hemodynamics, stroke volume and level of venous return to the heart.