The acute effect of a low dosage of pramipexole on severe idiopathic restless legs syndrome: an open-label trial

Neuropsychobiology. 2006;54(3):195-200. doi: 10.1159/000099947. Epub 2007 Feb 21.

Abstract

Background: Pramipexole is a D3 dopaminergic agonist that has shown a major effect on both sensory and motor manifestations of restless legs syndrome (RLS) in long-term trials. No data regarding the acute effect of low doses of pramipexole have been reported.

Objective: To evaluate the acute effect of a low dosage of pramipexole (0.125 mg) on sensory symptoms and motor signs of RLS and on the macro- and microstructure of sleep.

Methods: We initially recruited 13 patients affected by severe idiopathic RLS and included 10 of them in our study. For 2 consecutive nights the selected patients were evaluated. Pramipexole 0.125 mg was administered before the second night at 9:00 p.m. A visual analog scale was used to assess the sensory symptoms of RLS. The motor manifestations of RLS and the architecture of sleep were analyzed by polysomnography.

Results: After the acute administration of pramipexole, we observed a significant improvement of the sensory symptoms and motor signs of RLS. Several sleep macrostructure and microstructure parameters improved as well.

Conclusions: Our results suggest that low doses of pramipexole are effective in reducing sensory symptoms and motor signs of RLS, even after the first administration.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Benzothiazoles / administration & dosage*
  • Dopamine Agonists / administration & dosage*
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Male
  • Middle Aged
  • Pramipexole
  • Restless Legs Syndrome / drug therapy*
  • Severity of Illness Index
  • Sleep Stages / drug effects*
  • Treatment Outcome

Substances

  • Benzothiazoles
  • Dopamine Agonists
  • Pramipexole