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Heredodegenerative Disorders, Nervous System

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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

Creatine Metabolism in Rett Syndrome

NCT01198015

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

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Completed

NF1-Attention: Study of Children With Neurofibromatosis Type 1 Treated by Methylphenidate

NCT00169611

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +14 more
Locations: Laurence LION-FRANCOIS Lyon, France

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Completed

Dutasteride to Treat Spinal and Bulbar Muscular Atrophy (SBMA)

NCT00303446

Conditions: Bulbo-Spinal Atrophy, X-Linked, Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

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Completed

A Study of the Effectiveness and Safety of Risperidone Versus Placebo in the Treatment of Children With Autistic Disorder and Other Pervasive Developmental Disorders (PDD)

NCT00261508

Conditions: Asperger Syndrome, Autism Spectrum Disorder, Autistic Disorder, +15 more
Locations: Not specified

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Completed

Facial Expression Recognition of Emotion and Categorization of Emotional Words in Gilles de la Tourette's Syndrome

NCT00664300

Conditions: Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +11 more
Locations: CHU Clermont-Ferrand, France

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Completed

Postural Spirometry Changes in Ambulatory Myotonic Dystrophy Patients

NCT01242007

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
Locations: University Hospital of Nancy Vandœuvre-lès-Nancy, France

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Completed

A Study of KPS-0373 in Patients With Spinocerebellar Degeneration (SCD)

NCT01004016

Conditions: Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +8 more
Locations: Japan Japan

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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

A Study Investigating the Safety and Tolerability of Deferiprone in Patients With Friedreich's Ataxia

NCT00530127

Conditions: Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +12 more
Locations: Murdoch Children's Research Institute Victoria, Australia

Hospital Erasme Brussels, Belgium

McMaster University Hamilton, Ontario, Canada

Hospital Necker-Enfants Malades Paris, France

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Completed

Efficacy of Epoetin Alfa in Patients With Friedreich's Ataxia

NCT00631202

Conditions: Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +12 more
Locations: Dipartimento di Scienze Neurologiche Naples, Italy

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Heredodegenerative Disorders, Nervous System

Heredodegenerative Disorders, Nervous System trial results

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