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X-Linked Intellectual Disability

Clinical trial condition

X-Linked Intellectual Disability

Explore clinical trials studying X-Linked Intellectual Disability. Study availability and eligibility vary by location and protocol.

273 public trials 52 recruiting studies

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X-Linked Intellectual Disability trial results

Completed

Effects of Creatine Supplementation in Rett Syndrome

NCT01147575

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: Medical University Vienna, Dep. of Pediatric and Adolescent Medicine Vienna, Austria

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Completed

Metabolic Evaluation of Nutrition in Rett Syndrome

NCT00786071

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: University Hospital Maastricht Maastricht, Limburg, Netherlands

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Completed

A Single-Dose Study in Normal Volunteers to Assess the Safety, Tolerability and Pharmacokinetics of STX107

NCT00965432

Conditions: Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
Locations: Covance Clinical Research Unit Madison, Wisconsin, United States

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Completed

Functional Abilities in Rett Syndrome

NCT00630422

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +10 more
Locations: Faculdades Metropolitanas Unidas São Paulo, Brazil

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Completed

Advanced Grandparental Age as a Risk Factor for Autism

NCT00464477

Conditions: Asperger Syndrome, Autism Spectrum Disorder, Autistic Disorder, +15 more
Locations: University of Mississippi Medical Center Jackson, Mississippi, United States

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Completed

Study of the Pathogenesis of Rett Syndrome

NCT00004807

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
Locations: Not specified

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Completed

Effects of CX516 on Functioning in Fragile X Syndrome and Autism

NCT00054730

Conditions: Autism, Autism Spectrum Disorder, Autistic Disorder, +16 more
Locations: UC Davis-MIND Institute Sacramento, California, United States

RUSH-Presbyterian-St. Luke's Medical Center Chicago, Illinois, United States

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Completed

Phase I/II Study of Retroviral-Mediated Transfer of Iduronate-2-Sulfatase Gene Into Lymphocytes of Patients With Mucopolysaccharidosis II (Mild Hunter Syndrome)

NCT00004454

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +20 more
Locations: University of Minnesota Medical School Minneapolis, Minnesota, United States

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Completed

Study of Cardiac and Paroxysmal Abnormalities in Rett Syndrome

NCT00004773

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
Locations: Not specified

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Completed

Nutritional Aspects of Rett Syndrome

NCT00004656

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
Locations: Not specified

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