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Metabolic Diseases clinical trials

View clinical trials related to Metabolic Diseases.

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NCT ID: NCT00928473 Recruiting - Obesity Clinical Trials

The Danish Childhood Obesity Biobank

Start date: January 2009
Phase: N/A
Study type: Interventional

The Danish Childhood Obesity Biobank aims to produce a scientific platform for research in obesity: Bio-clinical data are collected from two cohorts - an obesity clinic cohort and a population-based cohort. The biobank thus facilitates translation between research and clinical practice of obesity treatment and related complications.

NCT ID: NCT00920972 Recruiting - Hemoglobinopathies Clinical Trials

Campath/Fludarabine/Melphalan Transplant Conditioning for Non-Malignant Diseases

Start date: December 2001
Phase: Phase 1/Phase 2
Study type: Interventional

The hypothesis for this study is that a preparative regimen that maximizes host immunosuppression without myeloablation will be well tolerated and sufficient for engraftment of donor hematopoietic cells. It is also to determine major toxicities from these conditioning regimens, within the first 100 days after transplantation.

NCT ID: NCT00707668 Recruiting - Metabolic Diseases Clinical Trials

Chung-ju Metabolic Disease Cohort (CMC) Study

Start date: May 2007
Phase: N/A
Study type: Observational

This is an observational study on the prevalence and incidence of diabetes and osteoporosis in a rural area of Korea.

NCT ID: NCT00687518 Recruiting - Clinical trials for Iron Metabolism Disorders

Effects of Intravenous Injection of Erythropoietin on Hepcidin Pharmacokinetics in Healthy Volunteers

HEPEPO
Start date: March 2008
Phase: N/A
Study type: Interventional

The aim of this study is to measure the variations of serum and urinary hepcidin levels following a single intravenous injection of erythropoietin in healthy volunteers. Hepcidin is a major regulator of iron homeostasis. It acts by binding on ferroportin, and limits cellular efflux of iron through enterocytes and macrophages. Anemia and hypoxia are known to modulate hepcidin synthesis. In these situations, erythropoietin synthesis is increased, so it can be postulated that erythropoietin could modulate hepcidin synthesis.

NCT ID: NCT00357331 Recruiting - Clinical trials for Osteoporosis, Postmenopausal

The Effects of Potassium Citrate on Bone Metabolism

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

Skeletal buffering of chronic acid loads may contribute to a significant amount of bone loss over time. Evidence from a few small short-term studies suggests that basic compounds, namely potassium citrate and potassium bicarbonate may reduce bone loss and improve bone density. The purpose of this study is to evaluate the effects of potassium citrate on bone metabolism. We hypothesize that administration of potassium citrate to postmenopausal women with osteopenia will reduce bone resorption and improve bone mineral density. Postmenopausal women with osteopenia (T score between -1.0 and -2.5) and no history of fracture will be randomized to either daily potassium citrate or placebo for one year. Primary outcomes will be markers of bone turnover, which will be measured over 12 months. Secondary outcomes will be bone mineral density, compliance, and adverse events.

NCT ID: NCT00237315 Recruiting - Clinical trials for Urea Cycle Disorders

Longitudinal Study of Urea Cycle Disorders

Start date: February 2006
Phase:
Study type: Observational

Urea cycle disorders (UCD) are a group of rare inherited metabolism disorders. Infants and children with UCD commonly experience episodes of vomiting, lethargy, and coma. The purpose of this study is to perform a long-term analysis of a large group of individuals with various UCDs. The study will focus on the natural history, disease progression, treatment, and outcome of individuals with UCD.