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Metabolism, Inborn Errors

Clinical trial condition

Metabolism, Inborn Errors

Explore clinical trials studying Metabolism, Inborn Errors. Study availability and eligibility vary by location and protocol.

2,496 public trials 457 recruiting studies

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Metabolism, Inborn Errors trial results

Completed

Studying Phosphorus Metabolism

NCT00066183

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, +14 more
Locations: National Institute of Dental And Craniofacial Research (NIDCR) Bethesda, Maryland, United States

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Completed

Estimation of the Carrier Frequency and Incidence of Smith-Lemli-Opitz Syndrome in African Americans

NCT00017732

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
Locations: National Institute of Child Health and Human Development (NICHD) Bethesda, Maryland, United States

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Completed

Iron Overload in African Americans

NCT00001455

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hemochromatosis, +6 more
Locations: National Institute of Child Health and Human Development (NICHD) Bethesda, Maryland, United States

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Completed

Study of Glycogen Storage Disease and Associated Disorders

NCT00001342

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +4 more
Locations: National Institute of Child Health and Human Development (NICHD) Bethesda, Maryland, United States

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Completed

Gene Therapy for Gaucher's and Fabry Disease Using Viruses and Blood-Forming Cells

NCT00001234

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +15 more
Locations: National Institute of Neurological Disorders and Stroke (NINDS) Bethesda, Maryland, United States

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Completed

Alpha-Galactosidase A Replacement Therapy for Fabry Disease

NCT00048906

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +20 more
Locations: National Institute of Neurological Disorders and Stroke (NINDS) Bethesda, Maryland, United States

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Completed

PET Scans in Normal Volunteers and Patients With Fabry Disease

NCT00005111

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +20 more
Locations: National Institute of Neurological Disorders and Stroke (NINDS) Bethesda, Maryland, United States

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Completed

New Cysteamine Eye Drops Formulation to Treat Corneal Crystals in Cystinosis

NCT00001736

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Genetic Diseases, Inborn, +4 more
Locations: National Eye Institute (NEI) Bethesda, Maryland, United States

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Completed

Vitamin Replacement in Abetalipoproteinemia

NCT00004574

Conditions: Abetalipoproteinemia, Ataxia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +20 more
Locations: National Heart, Lung and Blood Institute (NHLBI) Bethesda, Maryland, United States

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Completed

Study of Skeletal Disorders and Short Stature

NCT00001754

Conditions: Bone Diseases, Bone Diseases, Developmental, Carbohydrate Metabolism, Inborn Errors, +18 more
Locations: National Human Genome Research Institute (NHGRI) Bethesda, Maryland, United States

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