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OpenTrials
Completed

NCT Number: NCT00620165

Efficacy of Levetiracetam in Essential Tremor

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.

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Key information

Age range

25 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

VA Long Beach Healthcare System

Long Beach, California, 90822, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Levetiracetam

Drug

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.

Other names: keppra

Placebo

Drug

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 outcomes

  1. Performance on a 16-item tremor rating scale including degree of tremor, writing, pouring and feeding.

    Time frame: 12 weeks per treatment arm

Secondary outcomes

  1. Assessment of adverse side effects.

    Time frame: 12 weeks per arm

Sponsors and collaborators

Lead sponsor

Southern California Institute for Research and Education

Other

Registry information

Official study title

Efficacy of Levetiracetam in Patients With Essential Tremor

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
Feb 21, 2008
Registry last updated
Apr 17, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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