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Morbid Obesity clinical trials

View clinical trials related to Morbid Obesity.

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NCT ID: NCT02315105 Recruiting - Morbid Obesity Clinical Trials

Resolution of Comorbidities & Safety and Efficacy of Greater Curvature Plication in Obese Patients

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

The purpose of this study is to find out more about the safety and effectiveness of the Laparoscopic Greater Curvature Plication (LGCP) procedure in patients with obesity and related problems such as diabetes, hypertension, high cholesterol, mild obstructive sleep apnea, and joint problems. LGCP is a less invasive weight loss surgery procedure than some of the other weight loss surgeries and it is possible that there are fewer risks with this procedure than with the other weight loss surgeries. LGCP is considered an experimental procedure and this study is being done to look at the long-term outcomes.

NCT ID: NCT02295150 Recruiting - Morbid Obesity Clinical Trials

Prophylaxis of Venous Thromboembolism After Bariatric Surgery

Start date: March 2013
Phase: Phase 4
Study type: Interventional

This study is a prospective evaluation of the relationship between lean body weight and anti-Xa activity and 5700 International Units (IU) nadroparin 4 hours after subcutaneous administration in morbidly obese patients after bariatric surgery.

NCT ID: NCT02193529 Recruiting - Morbid Obesity Clinical Trials

Dietary Intake After Laparoscopic Sleeve Gastrectomy —a 5 Year Study

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

Weight reducing surgery is the only effective therapy for morbid obese patients. Sleeve gastrectomy is a popular choice for bariatric surgery because of less sequela. There is poor knowledge about the nutritional status inpatients after LSG. The aim of our study was to investigate the relationship between dietary intake and weight loss after LSG.

NCT ID: NCT02129296 Recruiting - Weight Loss Clinical Trials

Intragastric Balloon, Air Versus Fluid Filled: Randomized Prospective Study

Start date: September 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Gastric balloons are an evolving way of reducing weight. There are two types on the market, up to date. Air filled balloons seem to be more safe, and more tolerable.

NCT ID: NCT02128178 Recruiting - Pulmonary Embolism Clinical Trials

Laparoscopic Bariatric Surgery: Two Regimens of Venous Thromboprophylaxis: Prospective Randomized Study

Start date: November 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Obese patients undergoing bariatric surgery warrant VTE prophylaxis because they are at high risk for developing a fatal pulmonary embolism or postthrombotic syndrome. However, a consensus does not exist on the most effective prophylactic approach.

NCT ID: NCT02128165 Recruiting - Morbid Obesity Clinical Trials

Effect of Gastric Balloon in Morbid Obesity: Prospective Study

Start date: August 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to compare the efficacy of gastric balloon in weight reduction among two different categories of morbidly obese people.

NCT ID: NCT02118844 Recruiting - Morbid Obesity Clinical Trials

Laparoscopic Bariatric Surgery: Impact of Deep Neuromuscular Block on Surgical Conditions

BaChiBloPro1
Start date: July 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether deep neuromuscular blockade compared to moderate neuromuscular blockade may improve the surgical conditions in patients undergoing laparoscopic bariatric surgery.

NCT ID: NCT02077517 Recruiting - Morbid Obesity Clinical Trials

Stapled vs Hand Sewn Anastomosis in Roux en Y Gastric Bypass for Morbid Obesity: Randomized Clinical Trial

STAVHAS
Start date: January 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare postoperative complications between hand sewn and stapled anastomosis after performing Roux en Y-Gastric Bypass as a treatment for morbid obesity.

NCT ID: NCT02024542 Recruiting - Morbid Obesity Clinical Trials

Metabolic Responses to Bariatric Surgery

Start date: February 2011
Phase:
Study type: Observational

Research the genetic and biomechanical markers of human adipose tissue on patients with morbid obesity. Additional tissue/fluid collection is also gathered during the time of surgery.

NCT ID: NCT02017314 Recruiting - Morbid Obesity Clinical Trials

VAS Correlation With BMI

Start date: November 2013
Phase: Phase 4
Study type: Interventional

The aim of the study is to observe if any correlation between Body mass index and VAS values exists in patients who has gone under abdominal surgery. Group I : Patients with BMI<30 Group II: Patients with BMI between 30 and 34.9 Group III: Patients with BMI between 35 and 39.9 Group IV: Patients with BMI between 40 and 49.9 Group V : Patients with BMI >50 After the end of surgery patients will be extubated and in the recovery room morphine PCA (patient-controlled analgesia) treatment will be started according to their adjusted body weight. When VAS values over 4,10 mg/kg Paracetamol IV will be used as an escape treatment. VAS values and Delivery and Demand of the PCA and additional need for analgesics will be recorded in the first 48 hours.