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Clinical trial condition

Genetic Diseases, X-Linked

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

1,243 public trials 227 recruiting studies
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Genetic Diseases, X-Linked trial results

Completed

Pilot Study of a Suprachoroidal Retinal Prosthesis

NCT01603576

Conditions
Choroid Diseases, Choroideremia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
Locations
  • Nicta / Data61 Canberra, Australian Capital Territory, Australia
  • Centre for Eye Research Australia East Melbourne, Victoria, Australia
View Trial Details
Completed

Eplerenone for Subclinical Cardiomyopathy in Duchenne Muscular Dystrophy

NCT01521546

Conditions
Cardiomyopathies, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
Locations
  • Mattel Children's Hospital and David Geffen School of Medicine at UCLA Los Angeles, California, United States
  • Cincinnati Children's Hospital Medical Center Cincinnati, Ohio, United States
  • The Ohio State University Medical Center Columbus, Ohio, United States
View Trial Details
Completed

A Study With RO4917523 in Patients With Fragile X Syndrome

NCT01015430

Conditions
Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations
  • Sacramento, California, United States
  • Decatur, Georgia, United States
  • Chicago, Illinois, United States
  • Indianapolis, Indiana, United States
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Completed

New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization

NCT02885090

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations
  • Handicaps de l'Enfant - Pavillon Ste Marie, CHU St Jacques Besançon, France
  • Service de Neuropédiatrie, Hôpital St Jacques, CHU de Besançon Besançon, France
  • Unité de génétique, Groupe hospitalier Hôpital Flaubert Caen, France
  • Centre de Génétique Hôpital d'Enfants, CHU de Dijon Dijon, France
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Completed

A Device for Rapid, Painless, Bedside Muscle Evaluation of Children

NCT02340923

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations
  • Children's Hospital Colorado Aurora, Colorado, United States
  • Boston Children's Hospital Boston, Massachusetts, United States
  • Skulpt, Inc. Boston, Massachusetts, United States
  • St. Louis Children's Hospital St Louis, Missouri, United States
View Trial Details

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