Zonisamide for essential tremor: an evaluator-blinded study

Mov Disord. 2009 Feb 15;24(3):437-40. doi: 10.1002/mds.22418.

Abstract

In this evaluator-blinded open-treatment trial, subjects with moderate/severe upper limb essential tremor were titrated to 300 mg/day zonisamide, or adjusted to a lesser dose if symptoms warranted, as monotherapy or as adjunct to stable antitremor medication, followed by a 12-week extension phase. The primary efficacy outcome variables were blinded rater videotaped/drawing tremor score changes at the Treatment and Extension visits compared to Baseline, based on Fahn-Tolosa-Marin and Postural Tremor Scales. Subjects also rated Functional Disabilities. Primary outcomes showed reduced tremor scores at the Treatment (P < 0.00001, n = 25) and Extension (n = 16) visits, at mean doses of 252 and 225 mg/day, respectively. Subject ratings indicated 200 mg/day was superior to 100 mg/day, whereas 300 mg/day produced no additional benefit, but instead was associated with more adverse symptoms, most commonly somnolence, poor energy, imbalance, and altered taste. Future double-blind placebo-controlled trials are warranted.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aged
  • Anticonvulsants / therapeutic use*
  • Drug Administration Schedule
  • Essential Tremor / drug therapy*
  • Essential Tremor / physiopathology
  • Female
  • Humans
  • Isoxazoles / therapeutic use*
  • Male
  • Severity of Illness Index
  • Single-Blind Method
  • Upper Extremity / physiopathology
  • Zonisamide

Substances

  • Anticonvulsants
  • Isoxazoles
  • Zonisamide