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Genetic Diseases, Inborn

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Genetic Diseases, Inborn

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

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Genetic Diseases, Inborn trial results

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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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Characterisation of a Population of Adults Suffering From Cystic Fibrosis in a Belgian Reference Center

NCT07442682

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Cystic Fibrosis (CF), +13 more
Locations: Hôpital Erasme - HUB 808 route de Lennik 1070 Brussels Belgium Brussels, Belgium

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Applying Population Management Best Practices to Preventative Genomic Medicine Trial

NCT07053813

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Neoplasms, +1 more
Locations: Denver Health Denver, Colorado, United States

Kaiser Northwest Portland, Oregon, United States

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Digital Care for Holistic Health in Older Adults With Diabetes and Multimorbidity

NCT07310849

Conditions: Arthritis, Arthritis, Gouty, CKD, +23 more
Locations: Wugu District Public Health Center, New Taipei City, Wugu District, Taiwan

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Effect of Donor Diabetes and Other Factors on Corneal Transplant Endothelial Cell Loss and Success at 5 Years

NCT07217249

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Diseases, Corneal Dystrophies, Hereditary, +6 more
Locations: Georgia Eye Partners Atlanta, Georgia, United States

Price Vision Group Indianapolis, Indiana, United States

University of Iowa Hospitals and Clinics Iowa City, Iowa, United States

Kansas City Eye Clinic Overland Park, Kansas, United States

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Duchenne Muscular Dystrophy and the Viscoelastic Properties of Upper Limb Muscles

NCT07435116

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), Genetic Diseases, Inborn, +9 more
Locations: Sanko Unıversıty Gaziantep, Turkey (Türkiye)

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Registry of Patients With Hypophosphatasia

NCT02306720

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Hypophosphatasia, +5 more
Locations: Research Site Centennial, Colorado, United States

Research Site Hartford, Connecticut, United States

Research Site Tampa, Florida, United States

Research Site Decatur, Georgia, United States

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ATTRACT-52: Primary Care Cardiac Amyloidosis Screening in Ordu, Turkey

NCT07238426

Conditions: Amyloid Neuropathies, Amyloid Neuropathies, Familial, Amyloidosis, +15 more
Locations: Ordu University Faculty of Medicine, Department of Cardiology Ordu, Turkey (Türkiye)

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pCCLCHIM-p47 (Lentiviral Vector Transduced CD34 Plus Cells) in Patients With p47 Autosomal Recessive Chronic Granulomatous Disease (AR-CGD)

NCT06253507

Conditions: Autosomal Recessive, Chronic Disease, Chronic Granulomatous Disease, +15 more
Locations: National Institutes of Health Clinical Center Bethesda, Maryland, United States

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Investigation of the Relationship Between Executive Functions and Occupational Performance of Children With Duchenne Muscular Dystrophy

NCT06868784

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Executive Dysfunction, +10 more
Locations: Lokman Hekim University Ankara, Çankaya, Turkey (Türkiye)

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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