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| Found 50 studies with search of: | Cerebellar Degeneration |
| Rank | Status | Study | ||||
|---|---|---|---|---|---|---|
| 1 | Completed |
High-Dose Intravenous Immunoglobulin to Treat Cerebellar Degeneration
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| 2 | Withdrawn |
Intravenous Levetiracetam as First-line Anticonvulsive Treatment in Patients With Non-convulsive Status Epilepticus
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| 3 | Active, not recruiting |
Study to Determine the Safety and Tolerability of Varenicline (Chantix®) in Treating Spinocerebellar Ataxia Type 3
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| 4 | Recruiting |
Immunotherapy of the Paraneoplastic Syndromes
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| 5 | Active, not recruiting |
Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations
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| 6 | Completed |
Coenzyme Q10 in Adult-Onset Ataxia
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| 7 | Completed |
A Trial of 18F-AV-133 and 18F-AV-45 Positron Emission Tomography (PET)
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| 8 | Recruiting |
Neural Mechanisms Engaged in Control of Eye Movements
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| 9 | Completed |
A Study of KPS-0373 in Patients With Spinocerebellar Degeneration (SCD)
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| 10 | Completed |
Phase II Study of KPS-0373 in Patients With Spinocerebellar Degeneration (SCD)
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| 11 | Active, not recruiting |
A Phase II Double Blind Comparative Study of KPS-0373 in Patients With Spinocerebellar Degeneration (SCD)
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| 12 | Completed |
Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia
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| 13 | Not yet recruiting |
A New Method to Treat Hereditary Cerebellar Ataxia - Umbilical Cord Mesenchymal Stem Cells Transplantation
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| 14 | Recruiting |
Efficacy of Riluzole in Hereditary Cerebellar Ataxia
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| 15 | Not yet recruiting |
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias
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| 16 | Recruiting |
Biomarkers in Autosomal Dominant Cerebellar Ataxia
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| 17 | Completed |
Conjugate Pneumococcal Vaccine in Ataxia Telangiectasia (AT)
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| 18 | Active, not recruiting |
Characteristics of Episodic Ataxia Syndrome
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| 19 | Completed |
Phase 1 Trial of Idebenone to Treat Patients With Friedreich's Ataxia
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| 20 | Active, not recruiting |
Safety and Efficacy of Lithium Carbonate in Patients With Spinocerebellar Ataxia Type 3
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