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Body Weight clinical trials

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NCT ID: NCT01435603 Completed - Obesity Clinical Trials

Intervening in Diabetes With Healthy Eating, Activity, and Linkages To Healthcare - The I-D-HEALTH Study

I-D-HEALTH
Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare ways of giving advice and providing support to improve diet and physical activity in adult primary care patients with elevated body mass index and dysglycemia.

NCT ID: NCT01435278 Completed - Obesity Clinical Trials

Efficacy and Safety of Glucosanol in Maintaining Body Weight

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

To date, there is no clinical evidence on the efficacy and safety of Glucosanol in maintaining weight loss beyond the study duration of 12 weeks. The rationale for this open-label study is to assess the efficacy in preventing regain of loss body weight and safety of Glucosanol in subjects who are overweight or obese over a longer period after the initial weight loss.

NCT ID: NCT01423617 Completed - Overweight Clinical Trials

Efficacy and Safety of Zenoctil in Reducing Body Weight

Start date: July 2011
Phase: Phase 3
Study type: Interventional

The intention of the study is to evaluate the safety and potential body weight and body fat loss effects of a 12-week treatment with Zenoctil in a randomized, double-blind, placebo-controlled, parallel study conducted in Caucasian subjects. This study will also include a diet plan for each subject, calculated based on gender, age, and energy requirements; and adjusted to be slightly hypocaloric.

NCT ID: NCT01420029 Completed - Clinical trials for Low Birth Weight Neonates

Hospital-Based Phthalate Exposure in Very Low Birth Weight Neonates

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

In this observational pilot project, the investigators plan to document duration and sources of exposure to plasticizers in infants born at birth weights less than 1500 grams. The investigators will examine the association between exposure to plasticizers and outcomes such as performance on a neurological screening tool, extrauterine growth, and thyroid function.

NCT ID: NCT01417117 Completed - Ischemic Strokes Clinical Trials

Effect of Ischemic Strokes on Recovery From Intracerebral Hemorrhages

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

Intracerebral hemorrhage (ICH) occurs when small arteries in the brain rupture due to weakening by age, high blood pressure, and/or elevated cholesterol. In addition to artery rupture, recent data suggests that patients with ICH are also at risk for developing occlusion of arteries during the acute phase, called ischemic strokes. Data suggests these ischemic strokes can negatively impact patient outcomes. Diffusion weighted imaging (DWI) is a sequence on Magnetic Resonance Imaging (MRI) that is a sensitive marker for ischemic strokes in the brain. In this proposal, our primary aim is examine prospectively the effect DWI abnormalities have on functional outcomes in patients with ICH. Our hypothesis is that the DWI abnormalities found on MRI of the brain lead to worse functional outcomes in patients with ICH

NCT ID: NCT01407393 Completed - Clinical trials for Overweight and Obesity

Safety and Efficacy of Glucosanol in Reducing Body Weight in Overweight and Obese Subjects

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

Glucosanolâ„¢, the medical device to be investigated contains a proprietary plant extract that is a natural inhibitor of alpha-amylase and can reduce starch digestion. The rationale for this study is to confirm that Glucosanolâ„¢ ingestion will reduce body weight. A double-blind, randomized, placebo-controlled design has been chosen to assess the efficacy and safety of Glucosanolâ„¢ in subjects who are overweight and mildly obese.

NCT ID: NCT01395602 Completed - Body Weight Clinical Trials

Effect of Cabergoline on Weight and Glucose Tolerance

Start date: April 2002
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to determine the efficacy of cabergoline, a long-acting dopamine receptor agonist, on body weight and blood glucose in healthy obese adults. This is a randomized double-blind placebo controlled study. Twenty subjects each will be randomly assigned either placebo or cabergoline for 16 weeks. The effect of treatment on body weight and blood glucose and insulin levels will be compared in the treatment versus the placebo arm.

NCT ID: NCT01358890 Completed - Obesity Clinical Trials

Low-Carbohydrate Diet Intervention on Body Weight

Start date: May 2011
Phase: Phase 2/Phase 3
Study type: Interventional

- The primary aim of this study is to determine the adherence of low- carbohydrate among Chinese. - Then compare the effect of low-carbohydrate and traditional Chinese but restricted-calories diet on weight loss and metabolic traits.

NCT ID: NCT01355952 Completed - Obesity Clinical Trials

An Open-Label Pilot Trial of Alpha Lipoic Acid (ALA) for Weight Loss in Schizophrenia

ALA
Start date: May 2011
Phase: N/A
Study type: Interventional

The aim of this study is to collect pilot data to compare the effectiveness of treatment with Alpha Lipoic Acid (ALA) for reduction in body weight in 40 obese outpatients with schizophrenia or schizoaffective disorder in an open-label pilot trial. The investigators also plan to test the feasibility of utilizing ALA as a weight loss agent for obese outpatients with schizophrenia or schizoaffective disorder in terms of tolerability, schizophrenia symptoms, cognition and side effects. We have run a total of 12 non-diabetic participants and are now recruiting diabetic patients in hopes of comparing the two groups.

NCT ID: NCT01351506 Completed - Body Weight Clinical Trials

Effect of Body Weight Change to Surgical ICU Outcomes

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

Aims of study 1. Effect of daily weight change upto 7 days from ICU admission to outcome of treatment in 28 days 2. Determination cut point of maximum weight change to outcome treatment