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Deficiency Disease clinical trials

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NCT ID: NCT00657748 Withdrawn - Canavan Disease Clinical Trials

Lithium and Acetate for Canavan Disease

Start date: September 2009
Phase: Phase 2
Study type: Interventional

The aim of this study is to determine whether oral supplementation with lithium and acetate may improve the biological and clinical prognosis in patients with Canavan Disease.

NCT ID: NCT00162539 Completed - Deficiency Disease Clinical Trials

Relation Between Maternal Iodine Status and Prenatal Foetal Thyroid Dimension

Start date: October 2005
Phase: N/A
Study type: Interventional

Mother with severe Iodine deficiency are more likely to have neonates with further poor mental development . In order to select population which could benefit from iodine supplementation, ioduria has been tested but cannot be routinely practised. Strong background data suggest that iodine status could be antenatally correlated with foetal thyroid volume. The aim of that study is to examine correlation between these two parameter in a population of 130 healthy pregnant women.

NCT ID: NCT00016848 Completed - Healthy Clinical Trials

Effects of Dietary Carbohydrate and Fat on Hormones

Start date: June 2001
Phase: N/A
Study type: Observational

This study will try to determine if intake of dietary fats or carbohydrates influences the tendency to gain weight or accumulate body fat. It will examine how the hormones that regulate weight may change with a shift from a balanced diet to one that is low in fat or carbohydrate, irrespective of caloric intake. Men and women between the ages of 18 and 40 years with a body mass index of 30 to 49 kg/m2 may be eligible for this study. Candidates will be screened with a history, physical examination, blood tests and questionnaires regarding activity, prior diets, and eating patterns. Participants will follow two separate diet regimens for 5 days each. The first will be a balanced diet, and the second will be either a low-fat/high-carbohydrate diet or a low-carbohydrate/high-fat diet. The diets are not designed to produce weight loss. Participants will receive all their meals and snacks for the two diets from the National Institutes of Health and, for the first 3 days of each diet, will be seen as outpatients. For days 4 and 5 of each diet, they will be admitted to the Clinical Center and will undergo the following procedures: - Blood tests - Blood samples will be collected every 30 minutes over a 24-hour period through an indwelling catheter in the arm. A total of about 15 tablespoons will be drawn for each of the two diets. - 24-hour urine collection - One 24 hour urine collection will be done at home the day before admission to the Clinical Center, and the other will be done during the hospital stay. - Urinalysis and pregnancy test - A small urine sample will be taken and women will provide an additional sample for a pregnancy test. - Body measurements - Height and weight will be measured using scales. Body fat will be measured by two methods: skin fold thickness, measured with calipers in 5 separate places; and body circumference measurements, in which body parts are measured with a tape measure. - Bod pod measurement - Proportions of fat and non-fat tissue in body weight are measured while the participant sits in a capsule-like device for 5 minutes. - Bioelectric impedance analysis - Proportions of body fat are measured based on conduction of a small electric current. - Total body water estimate -The proportion of body weight that is water is determined, using a method that involves drinking a cup of a special kind of "heavy" water (deuterium) and then measuring the amount of heavy water in a urine sample taken after 4 hours. - Exercise - Participants will maintain their usual exercise routine, as it was before beginning the study.