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A trial of topiramate for patients with hereditary spinocerebellar ataxia.

Shiroh MiuraRyusuke SawadaAkiko YoritaHiroshi KidaTakashi KamadaYoshihiro Yamanishi
Published in: Clinical case reports (2023)
In an open pilot trial, six patients with various hereditary forms of spinocerebellar ataxia (SCA) were assigned to topiramate (50 mg/day) for 24 weeks. Four patients completed the protocol without adverse events. Of these four patients, topiramate was effective for three patients. Some patients with SCA could respond to treatment with topiramate.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • chronic kidney disease
  • peritoneal dialysis
  • randomized controlled trial
  • clinical trial
  • patient reported outcomes
  • study protocol