Wessel K, Langenberger K, Nitschke M F, Kömpf D
Department of Neurology, Medical University of Lübeck, Germany.
Arch Neurol. 1997 Apr;54(4):397-400. doi: 10.1001/archneur.1997.00550160041013.
To determine whether treatment with physostigmine can improve the conditions of patients with ataxia.
A double-blind crossover study with physostigmine was performed in 19 patients with degenerative cerebellar diseases.
Patients were selected from an ongoing prospective follow-up study at the university hospital in Lübeck, Germany.
Eleven patients with autosomal dominant cerebellar ataxia and 8 patients with idiopathic cerebellar ataxia.
Physostigmine was administered by using a transdermal system (patch) containing 30 mg of physostigmine as a base, of which about 6 mg is released during 24 hours along a diffusion gradient. Each treatment phase with the physostigmine patch or the placebo lasted 4 weeks, after which the treatment of patients was crossed over to the other phase.
Ataxia was documented and quantified by using a clinical score and posturographic measures.
Physostigmine patches had no significant effect on cerebellar symptoms.
Treatment with physostigmine does not improve the conditions of patients with ataxia.