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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.

12,672 public trials 2,143 recruiting studies

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Genetic Diseases, Inborn trial results

Completed

Pyruvate Kinase Deficiency Global Longitudinal Registry Substudy of Protocol AG348-C-008

NCT04995315

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +7 more
Locations: Massachusetts General Hospital Boston, Massachusetts, United States

Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico Milan, Italy

Universitair Medisch Centrum Utrecht Utrecht, Netherlands

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Completed

Wearable Skin Sensors to Assess Nocturnal Scratch Behavior

NCT03770858

Conditions: Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +9 more
Locations: Northwestern University Chicago, Illinois, United States

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Completed

Transplantation for Patients With Sickle Cell Disease From Mismatched Family Donors of Bone Marrow

NCT02757885

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +7 more
Locations: Children's Healthcare of Atlanta Atlanta, Georgia, United States

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Completed

Fetal Hemoglobin Induction Treatment Metformin

NCT02981329

Conditions: Anemia, Anemia, Hemolytic, Anemia, Hemolytic, Congenital, +9 more
Locations: Texas Children's Hospital Houston, Texas, United States

The University of Texas Health Science Center at Houston Houston, Texas, United States

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Completed

Clearance of 25-hydroxyvitamin D in Cystic Fibrosis

NCT03104855

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Digestive System Diseases, +5 more
Locations: University of Washington Seattle, Washington, United States

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Completed

Effectiveness of Upper Extremity Rehabilitation in pwFSHD (Patient With Facioscapulohumeral Dystrophia)

NCT05178706

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
Locations: Istanbul University-Cerrahpaşa Istanbul, Turkey (Türkiye)

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Completed

Making HD Voices Heard

NCT05268029

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +13 more
Locations: Huntington Study Group Rochester, New York, United States

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Completed

Comparative Study:Topison (Mometasone Furoate) Versus Two Others Mometasone Furoates

NCT04271007

Conditions: Atopic Dermatitis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dermatitis, +9 more
Locations: Dr Sérgio Sckalka Osasco, São Paulo, Brazil

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Completed

Clinical Intramuscular Gene Transfer of rAAV1.CMV.huFollistatin344 Trial to Patients With Duchenne Muscular Dystrophy

NCT02354781

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Nationwide Children's Hospital Columbus, Ohio, United States

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Completed

Assessment of Lifestyle, Blood Pressure, Cholesterol and Glycated Hemoglobin in a Specific Population

NCT04373863

Conditions: Arterial Hypertension, Behavior, Blood Glucose, High, +13 more
Locations: Augusto Theodoro de Figueiredo São Paulo, Brazil

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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