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Genetic Diseases, Inborn

Clinical trial condition

Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,613 public trials 2,162 recruiting studies

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Genetic Diseases, Inborn trial results

Completed

A Decentralized Clinical Trial to Promote Evidence-Based Care for Underserved Patients With Neurofibromatosis 1

NCT06262113

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +13 more
Locations: Massachusetts General Hospital Boston, Massachusetts, United States

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Completed

Applying Directly Observed Therapy to Hydroxyurea to Realize Effectiveness

NCT06264700

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +7 more
Locations: Lurie Children's Hospital Chicago, Illinois, United States

Nationwide Children's Hospital Columbus, Ohio, United States

Hasbro Children's Hospital Providence, Rhode Island, United States

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Completed

A Stress and Pain Self-management m-Health App for Adult Outpatients With Sickle Cell Disease

NCT04484272

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +7 more
Locations: University of Florida Gainesville, Florida, United States

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Completed

Efficacy and Safety of Pegzilarginase in Patients With Arginase 1 Deficiency

NCT03921541

Conditions: Amino Acid Metabolism, Inborn Errors, Arginase I Deficiency, Brain Diseases, +11 more
Locations: Harvey Pediatrics Rogers, Arkansas, United States

Children's Hospital of Orange County Orange, California, United States

Stanford University School of Medicine Stanford, California, United States

Children's National Medical Center Washington D.C., District of Columbia, United States

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Completed

WT1 in Colorectal Adenocarcinoma

NCT07778628

Conditions: Colonic Diseases, Colonic Neoplasms, Colorectal Cancer, +25 more
Locations: Faculty of Medicine, Sohag University Sohag, Egypt

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Completed

Retinitis Pigmentosa Clinical Measures and Repeatability Testing of Potential Outcome Measures

NCT03845218

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
Locations: National Institutes of Health Clinical Center Bethesda, Maryland, United States

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Completed

Improving Diagnosis and Clinical Management of Familial Hypercholesterolemia Through Integrated Machine Learning, Implementation Science, and Behavioral Economics

NCT05746247

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Hypercholesterolemia, +9 more
Locations: University of Pennsylvania Health System Philadelphia, Pennsylvania, United States

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Completed

A Study of CM310 in Subjects With Moderate-to-Severe Atopic Dermatitis

NCT06116565

Conditions: Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +9 more
Locations: Peking University People's Hospital Beijing, Beijing Municipality, China

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Completed

RISCA : Prospective Study of Individuals at Risk for SCA1, SCA2, SCA3, SCA6, SCA7

NCT01037777

Conditions: Ataxia, Brain Diseases, Central Nervous System Diseases, +12 more
Locations: Pitié Salpêtrière Hospital Paris, France

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Completed

Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex

NCT00001452

Conditions: Abnormalities, Multiple, Adrenal Gland Diseases, Adrenocortical Hyperfunction, +44 more
Locations: National Institutes of Health Clinical Center Bethesda, Maryland, United States

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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