Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Explore clinical trials studying Congenital, Hereditary, and Neonatal Diseases and Abnormalities. Study availability and eligibility vary by location and protocol.

18,369 public trials 3,138 recruiting studies

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Congenital, Hereditary, and Neonatal Diseases and Abnormalities trial results

Completed

Studies in Porphyria III: Heme and Tin Mesoporphyrin in Acute Porphyrias

NCT00004396

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +8 more
Locations: Rockefeller University Hospital New York, United States

University of Texas Medical Branch Galveston, Texas, United States

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Completed

The Safety and Effectiveness of Ganciclovir Plus Interferon Beta in Preventing the Return of Cytomegalovirus (CMV) of the Eyes in Patients With AIDS

NCT00002299

Conditions: AIDS-Related Opportunistic Infections, Acquired Immunodeficiency Syndrome, Amino Acid Metabolism, Inborn Errors, +32 more
Locations: USC Los Angeles, California, United States

UCI Med Ctr Orange, California, United States

Univ of California / San Diego Treatment Ctr San Diego, California, United States

Stanford at Kaiser / Kaiser Permanente Med Ctr San Francisco, California, United States

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Completed

Genetic Study of Patients With Primary Ciliary Dyskinesia

NCT00005650

Conditions: Abnormalities, Multiple, Ciliary Motility Disorders, Ciliopathies, +10 more
Locations: University of North Carolina School of Medicine Chapel Hill, North Carolina, United States

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Completed

Studies of Hereditary Hemorrhagic Telangiectasia

NCT00004648

Conditions: Cardiovascular Abnormalities, Cardiovascular Diseases, Congenital Abnormalities, +14 more
Locations: Not specified

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Completed

Phase II Study of Sodium Phenylbutyrate, Sodium Benzoate, Sodium Phenylacetate, and Dietary Intervention for Urea Cycle Disorders

NCT00004767

Conditions: Amino Acid Metabolism, Inborn Errors, Brain Diseases, Brain Diseases, Metabolic, +13 more
Locations: Not specified

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Completed

Phase I/II Study of Monoclonal Factor IX Concentrate for Factor IX Deficiency

NCT00004801

Conditions: Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +12 more
Locations: Not specified

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Completed

Phase I/II Study of Total Body Irradiation, Cyclophosphamide, and Fludarabine Followed by Alternate Donor Hematopoietic Cell Transplantation in Patients With Fanconi's Anemia

NCT00005898

Conditions: Anemia, Anemia, Aplastic, Anemia, Hypoplastic, Congenital, +12 more
Locations: University of Minnesota Cancer Center Minneapolis, Minnesota, United States

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Completed

Phase I Study of Ex Vivo Liver-Directed Gene Therapy for Familial Hypercholesterolemia

NCT00004809

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Dyslipidemias, +13 more
Locations: Not specified

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Completed