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

Status: Completed

Phase of Trial: Phase III

Latest Information Update: 09 Nov 2021

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At a glance

Drugs Pramipexole (Primary)
Indications Restless legs syndrome
Focus Therapeutic Use
Sponsors Boehringer Ingelheim

Most Recent Events

09 Mar 2010 Patient numbers amended from (305) to (306) as reported by ClinicalTrials.gov.
22 Jul 2009 Actual patient number (305) added as reported by ClinicalTrials.gov.
22 Jul 2009 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.

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