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Genetic Diseases, X-Linked

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

Safety, Tolerability and Effects of L-Arginine in Boys With Dystrophinopathy on Corticosteroids

NCT01388764

Conditions: Becker's Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, +10 more
Locations: Massachusetts General Hospital Boston, Massachusetts, United States

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Completed

Sweat Duct Imaging in Mother/Newborn Dyads

NCT01342133

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
Locations: Washington University School of Medicine St Louis, Missouri, United States

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Completed

Medical Record Review of Hypohidrotic Ectodermal Dysplasia Clinical Phenotype

NCT01398397

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Edimer Pharmaceuticals Cambridge, Massachusetts, United States

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Completed

Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia: Intrafamilial Variation

NCT01386775

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
Locations: Hilton Garden Inn St. Louis Shiloh/O'Fallon O'Fallon, Illinois, United States

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Completed

Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected by Hypohidrotic Ectodermal Dysplasia - A

NCT01293565

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +9 more
Locations: University of California San Francisco, California, United States

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Completed

Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia (ECP-012)

NCT01629927

Conditions: Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Center for Rare Diseases Burgos, Spain

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Completed

Fabry and Stroke Epidemiological Protocol (FASEP): Risk Factors In Ischemic Stroke Patients With Fabry Disease

NCT01182818

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +23 more
Locations: Department of Neurology, Kreiskrankenhaus Altenburg Altenburg, Germany

Dept. of Neurology, Vivantes Netzwerk für Gesundheit GmbH, Klinikum Neukölln Berlin, Germany

Department of Neurology, Allgemeines Krankenhaus Celle Celle, Germany

Department of Neurology, Klinikum Chemnitz gGmbH Chemnitz, Germany

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Completed

Open Label Study Investigating Safety and Efficacy of NPL2009 50 mg - 150 mg on Prepulse Inhibition Tests and Continuous Performance Tasks, Adults With Fragile X Syndrome

NCT00637221

Conditions: Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: MIND Institute Sacramento, California, United States

Rush University Medical Centre Chicago, Illinois, United States

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Completed

Anderson-Fabry Disease in Chronic Kidney Disease Patients Not on Renal Replacement Therapy

NCT00728364

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +32 more
Locations: Klinikum Wels-Grieskirchen Wels, Upper Austria, Austria

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Completed

Six Month Study of Gentamicin in Duchenne Muscular Dystrophy With Stop Codons

NCT00451074

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Neuromuscular Research Institute - Scottsdale Healthcare Hopsital at Shea Scottsdale, Arizona, United States

University of Kansas Kansas City, Kansas, United States

The Research Institute at Nationwide Children's Hospital Columbus, Ohio, United States

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Genetic Diseases, X-Linked

Genetic Diseases, X-Linked trial results

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