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Swiss Restless Legs Syndrome Trial (SRLS) A Double-blind, Randomised, Crossover Trial Investigating the Efficacy and Safety of the Dopamine Agonist Pramipexole (Sifrol®, 0.25-0.75 mg Per Day) Versus Levodopa / Benserazide (Madopar® DR, 125-375 mg Per Day) in Patients With Restless Legs Syndrome

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Trial Profile

Swiss Restless Legs Syndrome Trial (SRLS) A Double-blind, Randomised, Crossover Trial Investigating the Efficacy and Safety of the Dopamine Agonist Pramipexole (Sifrol®, 0.25-0.75 mg Per Day) Versus Levodopa / Benserazide (Madopar® DR, 125-375 mg Per Day) in Patients With Restless Legs Syndrome

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 08 Nov 2013

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At a glance

  • Drugs Pramipexole (Primary) ; Levodopa/benserazide
  • Indications Restless legs syndrome
  • Focus Therapeutic Use
  • Acronyms SRLS
  • Sponsors Boehringer Ingelheim Pharmaceuticals

    • Most Recent Events

    • 01 Nov 2011 Results published in the Swiss Medical Weekly.
    • 04 Sep 2006 Status change
    • 18 Nov 2005 New trial record.
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