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Clinical trial

A Randomized, Double-blind, Placebo Controlled Dose Titration Trial With 0.125-0.75 mg Pramipexole (Sifrol®) Orally q.n. to Investigate the Safety and Efficacy in Out-patients With Idiopathic Restless Legs Syndrome for 6 Weeks

NCT00654498 is registered in ClinicalTrials.gov with Boehringer Ingelheim as lead sponsor.

NCT NCT00654498
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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Double-blind, Placebo Controlled Dose Titration Trial With 0.125-0.75 mg Pramipexole (Sifrol®) Orally q.n. to Investigate the Safety and Efficacy in Out-patients With Idiopathic Restless Legs Syndrome for 6 Weeks
Lead sponsor
Boehringer Ingelheim
Phase
Phase 3
Overall status
Completed
Start date
April 30, 2008
Completion date
June 30, 2009
Enrollment
306 (actual)
Sites
16

Conditions

As the registry lists them; a condition with its own page is linked.

restless legs syndrome