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Weight Loss clinical trials

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NCT ID: NCT00394667 Completed - Obesity Clinical Trials

Effect of Tesofensine on Weight Reduction in Patients With Obesity.

Start date: September 2006
Phase: Phase 2
Study type: Interventional

Purpose: To evaluate the efficacy on weight reduction, metabolic parameters and safety of tesofensine versus placebo in obese patients

NCT ID: NCT00377026 Completed - Obesity Clinical Trials

FirstWIND: Weight Loss Interventions After Delivery

Start date: September 2006
Phase: N/A
Study type: Interventional

This a pilot intervention study in which postpartum women will be randomized to receive a 6-month postpartum weight loss intervention or usual care.

NCT ID: NCT00375492 Completed - Clinical trials for Type 2 Diabetes Mellitus

Effect on Weight Loss of Exenatide Versus Placebo

Start date: September 2006
Phase: Phase 3
Study type: Interventional

This trial is designed to compare the effects of twice-daily exenatide and twice-daily placebo on weight loss. This trial will evaluate overweight and obese subjects with type 2 diabetes who have inadequate glycemic control with metformin, sulfonylurea, or metformin plus a sulfonylurea. Subjects will be treated with exenatide or placebo in addition to their current oral antidiabetes agent regimen and participate in a lifestyle modification program.

NCT ID: NCT00373971 Completed - Hip Fracture Clinical Trials

Preventing Loss of Weight, Fat Free Mass and Activities of Daily Living

Start date: November 1995
Phase: N/A
Study type: Interventional

Malnutrition of elder orthopaedic patients leads to weight loss and loss of fat free mass. Changes in the individual’s nutritional status and body composition may adversely affect the patient’s postoperative level of activity. Aim. Thus, the purpose of the present study is to report changes in postoperative weight, FFM and functions vital to daily living in a group of elder orthopaedic patients that were actively involved in their nutritional care during the hospital stay.

NCT ID: NCT00357344 Completed - Weight Loss Clinical Trials

Study of Effects From Gastric Bypass Weight Loss on Brain Tissue

Start date: May 24, 2006
Phase: N/A
Study type: Observational

This study will evaluate how large, intentional weight reduction affects the human brain and possible ways to reverse the changes associated with excess body weight. Subtle changes in some brain regions occur in people who are overweight. Such changes may involve the regulation of eating behavior, though it is not clear whether the changes were present before weight gain or are a consequence. Magnetic resonance imaging (MRI) will be used to study local structures of the brain. Patients ages 18 to 45 who are undergoing gastric bypass surgery and who are not pregnant or breastfeeding may be eligible for this study. A study group of lean participants will serve as controls. Patients will visit the Phoenix Indian Medical Center for about 3 days at a time for tests. They will have a medical examination, electrocardiogram, and tests of blood and urine. Questionnaires they will complete involve patients' moods and possible influence on eating behaviors, as well as food preferences. A taste test, smell test, and assessment of decision-making processes will be conducted. An oral glucose tolerance test involves a needle placed intravenously (IV) in the arm, for drawing blood after patients drink a sugar solution. The test takes about 3-1/2 hours, with six blood samples taken (about 2 tablespoons total). A meal test also includes use of an IV line. After patients consume a liquid meal, blood will be collected to analyze levels of blood sugar and hormones. For the DEXA scan, which measures body composition, patients will lie still while low-dose X-rays are used for 5 to 10 minutes. Urine will be collected for 1 whole day, to measure cortisol, a hormone. The MRI scan uses a strong magnetic field to obtain images of body organs and tissues. Patients having any metal in the body that may interfere with the scanning machine should not have this test. For the MRI procedure, patients will lie on a table that slides into the enclosed tunnel of the scanner and be asked to lie still. Patients will be able to communicate with the MRI staff at all times during the scan, and they may ask to be removed from the machine at any time.

NCT ID: NCT00352157 Completed - Weight Loss Clinical Trials

Effect of Revival Soy on Weight Loss and Skin, Hair, and Nails in Premenopausal Women

Start date: July 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if dietary consumption of Revival Soy can improve the appearance of the skin, hair, and finger nails and support weight loss in overweight, premenopausal women.

NCT ID: NCT00349635 Completed - Obesity Clinical Trials

A Controlled-Study on the Effect of a Combination of Fenofibrate and Metformin on Weight Loss and Weight Loss-Maintenance, in Obese Patients.

Start date: October 2004
Phase: Phase 2
Study type: Interventional

To investigate the effect on body weight of a combination fenofibrate and metformin on top of a moderate balanced calorie-deficit diet.

NCT ID: NCT00315146 Completed - Obesity Clinical Trials

Optimizing Body Composition for Function in Older Adults

Start date: April 2006
Phase: Phase 4
Study type: Interventional

The purpose of this pilot study is to compare two strategies intended to improve the health of overweight older adults by improving body composition. One strategy, resistance training, is designed to preserve skeletal muscle mass. The other strategy, the use of a PPAR-γ agonist, is designed to enhance the loss of fat from visceral and skeletal depots. These strategies will be used in conjunction with a hypocaloric diet and will be compared to a hypocaloric diet alone to determine if either of these strategies are superior in reducing visceral fat and preserving muscle mass.

NCT ID: NCT00297180 Completed - Obesity Clinical Trials

Weight Loss In Obese Subjects Taking Either GW869682 Or Placebo 3 Times Per Day For 12 Weeks

Start date: January 2006
Phase: Phase 2
Study type: Interventional

GW869682 causes glucose to be excreted in the urine. The purpose of this study is to see whether enough calories from glucose are excreted in the urine to cause weight loss.

NCT ID: NCT00292773 Completed - Obesity Clinical Trials

Weight Reduction Surgery and Ovarian Function

Start date: February 2006
Phase: N/A
Study type: Observational

This study will investigate the role of weight reduction surgery on the reproductive performance of obese women with ovulation problems. It is hypothesized that surgery offered when other methods of weight reduction have failed, may help restore ovulation.