Efficacy of Levetiracetam in Essential Tremor
Primary Purpose
Essential Tremor
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
levetiracetam
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Essential Tremor focused on measuring tremor, writing, feeding, pouring
Eligibility Criteria
Inclusion Criteria:
- History of tremor for 5 or more years
- No other neurological problems
Exclusion Criteria:
- Prior stroke or other neurological disease, psychiatric problems
- History of renal disease
- Pregnancy
Sites / Locations
- VA Long Beach Healthcare System
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
1
2
Arm Description
Outcomes
Primary Outcome Measures
Performance on a 16-item tremor rating scale including degree of tremor, writing, pouring and feeding.
Secondary Outcome Measures
Assessment of adverse side effects.
Full Information
NCT ID
NCT00620165
First Posted
February 11, 2008
Last Updated
April 16, 2009
Sponsor
Southern California Institute for Research and Education
1. Study Identification
Unique Protocol Identification Number
NCT00620165
Brief Title
Efficacy of Levetiracetam in Essential Tremor
Official Title
Efficacy of Levetiracetam in Patients With Essential Tremor
Study Type
Interventional
2. Study Status
Record Verification Date
April 2009
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
March 2008 (Actual)
Study Completion Date
March 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Southern California Institute for Research and Education
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Essential tremor poses one of the greatest therapeutic challenges to neurologists. This study will examine the effectiveness of the drug, levetiracetam or keppra, for the treatment of essential tremor.
Detailed Description
Currently available pharmacological treatments for essential tremor are hampered by relatively low efficacy and intolerable side effects. Recent evidence indicates that levetiracetam (LEV) may modulate the dopaminergic system. In this regard LEV has been shown to reduce L-dopa-induced dyskinesias, tardive dyskinesia and myoclonus, and is relatively well-tolerated in the elderly. Previous studies examined the efficacy of LEV for the treatment of essential tremor. However, these were either open label or relatively short duration studies. A longer term study of LEV for the treatment of essential tremor is therefore warranted. In this randomized, double-blind, placebo-controlled crossover study, ten subjects with essential tremor will be randomly assigned to receive either LEV up to a maximum dose of 3000 milligrams (mg) per day or placebo. Study drug will be titrated up over 6 weeks and continued at 1500 mg twice daily for an additional 6 weeks. Following a 4 week washout period subjects will cross over to the other arm and continued for an additional 12 weeks. Subjects will be evaluated monthly by a blinded examining neurologist and research coordinator. At each study visit subjects will receive a neurological examination and will be evaluated using a 16-item scale for tremor and medication side effects. The data derived from study drug vs. placebo groups will be compared using the Mann-Whitney U and Wilcoxon W tests.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Essential Tremor
Keywords
tremor, writing, feeding, pouring
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
levetiracetam
Other Intervention Name(s)
keppra
Intervention Description
Subjects will receive levetiracetam titrated up over 6 weeks to a maximum dose of 3000 milligrams (mg) per day, and then continue at 1500 mg twice daily for an additional 6 weeks.
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
Subjects will receive identical placebo titrated up over 6 weeks to a maximum daily dose, and then continue twice daily for an additional 6 weeks.
Primary Outcome Measure Information:
Title
Performance on a 16-item tremor rating scale including degree of tremor, writing, pouring and feeding.
Time Frame
12 weeks per treatment arm
Secondary Outcome Measure Information:
Title
Assessment of adverse side effects.
Time Frame
12 weeks per arm
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
History of tremor for 5 or more years
No other neurological problems
Exclusion Criteria:
Prior stroke or other neurological disease, psychiatric problems
History of renal disease
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven S Schreiber, MD
Organizational Affiliation
Southern California Institute for Research and Education
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Long Beach Healthcare System
City
Long Beach
State/Province
California
ZIP/Postal Code
90822
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Efficacy of Levetiracetam in Essential Tremor
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