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Heredodegenerative Disorders, Nervous System

Clinical trial condition

Heredodegenerative Disorders, Nervous System

Explore clinical trials studying Heredodegenerative Disorders, Nervous System. Study availability and eligibility vary by location and protocol.

1,877 public trials 411 recruiting studies

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Heredodegenerative Disorders, Nervous System trial results

Completed

Study to Determine the Safety and Tolerability of Varenicline (Chantix®) in Treating Spinocerebellar Ataxia Type 3

NCT00992771

Conditions: Ataxia, Brain Diseases, Central Nervous System Diseases, +14 more
Locations: University of California - Los Angeles Los Angeles, California, United States

University of Florida Gainesville, Florida, United States

University of South Florida Tampa, Florida, United States

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Completed

Transcorneal Electrical Stimulation Therapy for Retinal Disease

NCT00804102

Conditions: Arterial Occlusive Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +35 more
Locations: Not specified

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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

Memory Disorders Registry

NCT00654563

Conditions: Alzheimer Disease, Alzheimer's Disease, Basal Ganglia Diseases, +24 more
Locations: Cedars-Sinai Medical Center Los Angeles, California, United States

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Completed

Clinical Trial of Pirfenidone in Adult Patients With Neurofibromatosis 1

NCT00754780

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +16 more
Locations: Not specified

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Completed

Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)

NCT00004306

Conditions: Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +15 more
Locations: University of Texas Medical Branch at Galveston Galveston, Texas, United States

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Completed

Topical Rapamycin Therapy to Alleviate Cutaneous Manifestations of Tuberous Sclerosis Complex (TSC) and Neurofibromatosis I (NF1)

NCT01031901

Conditions: Angiofibroma, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +23 more
Locations: The University of Texas Health Science Center Houston, Texas, United States

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Completed

DM1 Heart Registry - DM1 Respiratory Registry

NCT01136330

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, +16 more
Locations: Pitié Salpêtrière Hospital Paris, Île-de-France Region, France

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Completed

Riluzole in Huntington's Disease

NCT00277602

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +13 more
Locations: Not specified

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Completed

To Evaluate the Safety and Efficacy of GC1111 (Recombinant Human Iduronate-2-sulfatase) in Hunter Syndrome Patients

NCT01301898

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +22 more
Locations: Samsung Medical Center Seoul, Irwon-dong, Gangnam-Gu, South Korea

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Heredodegenerative Disorders, Nervous System

Heredodegenerative Disorders, Nervous System trial results

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