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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
Southern California Institute for Research and Education
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Essential Tremor focused on measuring tremor, writing, feeding, pouring

Eligibility Criteria

25 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
February 11, 2008
Last Updated
April 16, 2009
Sponsor
Southern California Institute for Research and Education
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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

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Efficacy of Levetiracetam in Essential Tremor

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