drugset / Trial / NCT00275457

Efficacy and Safety of Pramipexole (PPX) in Moderate to Severe Idiopathic Restless Legs Syndrome (RLS) Patients

NCT00275457

Phase 3 Completed 346 enrolled Boehringer Ingelheim
RandomizedSingle-groupDouble-blindTreatment

Summary

To evaluate safety and efficacy of pramipexole in the treatment of patients suffering from moderate to severe RLS over 6 weeks under double blinded conditions followed by a 46 week open label or double blind extension.

Timeline

Start
2002-10
Primary completion
2004-04
Completion
2004-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramipexole Unknown Oral