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Obesity clinical trials

View clinical trials related to Obesity.

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NCT ID: NCT01488643 Recruiting - Obesity Clinical Trials

Observational Study on Obese Patients During General Anesthesia

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

There is increased frequency of asthma in obese patients. This study is trying to find out if there is a difference in the presence of bronchospasm during anesthesia in obese and non obese patients.

NCT ID: NCT01477957 Recruiting - Obesity Clinical Trials

The Effect of Bariatric Surgery on Insulin Sensitivity and Energy Metabolism

BARIA-DDZ
Start date: September 2012
Phase:
Study type: Observational

The purpose of this study is: 1. To explore to what extent insulin sensitivity, energy metabolism and ectopic lipid storage can be improved by bariatric surgery 2. To explore to what extent hepatic and muscular disorders of energy metabolism occur in patients with obesity (degree 2-3) 3. To explore whether the steato liver occurring in patients with obesity (degree 2-3) is associated with the degree of liver inflammation

NCT ID: NCT01471275 Recruiting - Clinical trials for Type 2 Diabetes Mellitus ;Obesity,High Triglycerides;TCM

Chinese Medicine Treatment of Obesity With Type 2 Diabetes, Dyslipidemia

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

With metformin for the control, evaluate the safety and efficacy of Jiangtangtiaozhi decoction in treatment of obesity with type 2 diabetes, dyslipidemia

NCT ID: NCT01470534 Recruiting - Obesity Clinical Trials

Mechanisms Underlying Postoperative Insulin Resistance and Inflammation

Start date: November 2011
Phase: Phase 4
Study type: Interventional

Having an operation places an enormous burden on the body, leading to the development of inflammation and so called 'insulin resistance'. Insulin resistance means the body is unable to respond to important hormones that control use of energy. Recent studies have shown that patients who develop 'higher' insulin resistance and inflammation have more serious complications and take longer to recover after surgery. The investigators do not know what controls the development of insulin resistance and inflammation after surgery. Similarly, the investigators do not know why certain patients develop much more insulin resistance and inflammation than others, even though they have the same operation. The main purpose of the study is to try to find out which patients are prone to developing greater 'amounts' of insulin resistance and inflammation. The investigators also want to find out whether the investigators can reduce the 'amount' of insulin resistance and inflammation in these patients (for example by giving them carbohydrate [sugar-based] drinks before surgery - these have been shown to reduce insulin resistance in some patient groups). Information from this study should improve the way the investigators prepare patients before surgery and this should help to improve patient outcomes following surgery (by reducing complications and speeding recovery after major surgery).

NCT ID: NCT01470378 Recruiting - Obesity Clinical Trials

Manual Lymphatic Drainage in Women Undergone to Thigh Lifting

Thight_lift
Start date: January 2011
Phase: Phase 1
Study type: Interventional

This study will investigate the subcutaneous tissue changes in the lymphedema found after thigh surgery, by circumferential measure of thr thighs and by magnetic resonance imaging verifying the effects of postoperative lymphatic drainage.

NCT ID: NCT01468116 Recruiting - Obesity Clinical Trials

The Effect of Roux-en-Y Gastric Bypass on Mitochondrial Function in Type 2 Diabetes

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

Roux-en-Y gastric bypass (RYGB) surgery induces resolution of type 2 diabetes, often within days after surgery and before significant weight loss. The aim of this study is to investigate whether changes in mitochondrial function contributes to the early improvement of type 2 diabetes after RYGB.

NCT ID: NCT01463904 Recruiting - Diabetes Clinical Trials

Single-Anastomosis Duodeno-Ileal Bypass With Sleeve Gastrectomy (SADI-S) for the Treatment of Morbid Obesity and Its Metabolic Complications

SADI-S 250
Start date: April 2007
Phase: N/A
Study type: Observational

Single-Anastomosis Duodeno-Ileal Bypass with Sleeve Gastrectomy is a modified and simplified duodenal switch. It is performed on morbid obese patients and severe T2DM patients with obesity, and a proper weight loss is expected as well as a decrease in the cardiac risk and a remission of T2DM. A lower complication rate than for duodenal switch is expected.

NCT ID: NCT01455077 Recruiting - Obesity Clinical Trials

Portable Monitoring Device for the Diagnosis of Sleep Apnea in Obese Patients

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

Introduction The portable monitoring system (PMS) recording of cardiopulmonary parameters (level III of ASDA) has been validated in subjects with high probability of Obstructive Sleep Apnea (OSA) without comorbidities. However, there is not any study evaluating this system when OSA is associated with morbid obesity, so the validation of PMS will be very useful in order to properly work-up this highly risk population. Objective: To evaluate the accuracy of level III type of PMS - Stardustâ„¢" (STD), on patients with level II and III of obesity and high clinical suspicion of OSA. Methods:Participants with BMI > 35 kg/m2 and with suspicion of OSA will consecutively be selected from an Outpatients Sleep Clinic of UNIFESP. They will be randomized for the following order of recordings: 1) STD at home for 1 night 2) STD in the sleep lab simultaneous to PSG. AHI will be taken for subsequent analysis:a) AHI PSG b) AHI STD -lab and c) AHI STD- home.

NCT ID: NCT01448785 Recruiting - Obesity Clinical Trials

Abilitiâ„¢ Treatment in Obese Subjects

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

The main objective of this post-market surveillance study is to compare the subject's weight loss and quality of life, and device safety performance of the abiliti System and the adjustable gastric banding therapies in obese to morbidly obese subjects.

NCT ID: NCT01443143 Recruiting - Obesity Clinical Trials

Blood Glucose Stability and Variability on Two Diets

Start date: December 2010
Phase: N/A
Study type: Interventional

This investigation will examine the effects of consuming a structured, portion-controlled, low-glycemic index diet (commercially available as the Nutrisystem-D program) on several indicators of glycemic stability and variability among participants with type 2 diabetes. Results on the portion-controlled diet will be compared with those on participants' usual diets in a randomized cross-over trial. The investigators expect that participants will exhibit greater glycemic stability (e.g., more time in euglycemic range) and less glycemic variability (e.g., smaller mean amplitude of glycemic excursions) while consuming the Nutrisystem D program, as compared with their usual diet.