Double-blind, placebo-controlled, cross-over trial of allopurinol as add-on therapy in childhood refractory epilepsy

Brain Dev. 1996 Jan-Feb;18(1):50-2. doi: 10.1016/0387-7604(95)00110-7.

Abstract

We report the results of a double-blind, placebo-controlled cross-over trial with allopurinol as add-on therapy in childhood refractory epilepsy. Seventeen patients received allopurinol and matched placebo for 12 weeks in 2 doses (10 mg/kg/day during the first week and 15 mg/kg/day thereafter with a washout period of 2 weeks between treatment phases. The total number of seizures was reduced by 50-98% in 4 patients (23.5%) and by 25-49% in another 4 (23.5%). However, the number of seizures remained unchanged in 5 patients (29.4%) and worsened in 4 (23.5%). Adverse side effects (17.6%) were generally mild and transient, suggesting that allopurinol is well-tolerated. A mean follow-up of 10 months of the responders did not show any relevant efficacy of allopurinol as an adjuvant therapy for refractory epilepsy, even at high doses.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Adolescent
  • Adult
  • Allopurinol / administration & dosage*
  • Anticonvulsants / administration & dosage
  • Child
  • Cross-Over Studies
  • Double-Blind Method
  • Drug Resistance
  • Drug Therapy, Combination
  • Enzyme Inhibitors / administration & dosage*
  • Epilepsy / drug therapy*
  • Follow-Up Studies
  • Humans
  • Placebos
  • Uric Acid / blood

Substances

  • Anticonvulsants
  • Enzyme Inhibitors
  • Placebos
  • Uric Acid
  • Allopurinol