The Effect of Levetiracetam (Keppra) on the Treatment of Tremor in Multiple Sclerosis
NCT ID: NCT00430599
Last Updated: 2015-10-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
20 participants
OBSERVATIONAL
2007-02-28
2009-09-30
Brief Summary
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Detailed Description
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Cerebellar tremor and cerebellar gait instability are present in up to 70% of chronic MS patients and account for a significant amount of clinical morbidity. Cerebellar tremor is a major therapeutic problem in MS since currently there are no effective treatments. To date medical therapies including propranolol, clonazepam, carbamazepine, isoniazid, phenobarbitone, ondansetron, topiramate, gabapentin and cannabis have all been studied with little sustained benefit. More radical surgical treatments including thalamotomy and Deep Brain Stimulation have also been attempted.
However, a recent pilot study, with a small number of patients, suggested that Keppra (Levetiracetam) is effective in treating MS tremor. This study relied upon a rather subjective assessment of tremor and did not assess patients using quantitative physiological measures.
This protocol involves a collaboration between a clinical neurologist, with a recognised expertise in MS, and a research group with an established expertise in the electrophysiological and pharmacological investigation of human tremor11. The protocol describes a study, in MS patients, designed to establish whether Keppra (Levetiracetam) produces:
1. Physiologically measurable reduction in tremor;
2. Subjective and qualitative reduction in tremor;
Conditions
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Study Design
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CASE_CROSSOVER
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
2. Clinical evidence of Cerebellar Tremor.
3. Aged 18-60
Exclusion Criteria
2. Evidence of resting tremor, or Holmes (rubral) tremor
3. Pregnant or breast feeding mothers
4. Patients with inadequate understanding of the English language to comprehend the patient information sheet
5. Evidence of any significant renal impairment
6. History of epilepsy
18 Years
60 Years
ALL
No
Sponsors
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Newcastle-upon-Tyne Hospitals NHS Trust
OTHER
Responsible Party
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Principal Investigators
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Dr P Nichols, MRCP, DPhil
Role: PRINCIPAL_INVESTIGATOR
Newcastle NHS Hospitals Trust
Locations
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Sir James Spence Institute, Royal Victoria Infirmary
Newcastle, Tyne and Wear, United Kingdom
Countries
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Other Identifiers
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3384
Identifier Type: -
Identifier Source: org_study_id
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