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Sifrol (Pramipexole) Onset of Action and Impact: a 12-weeks Observational Study in Patients With Primary Restless Legs Syndrome

Restless Legs Syndrome Clinical Trial

Official title:
Sifrol Onset of Action and Impact: a 12-weeks Observational Study in Patients With Primary RLS

Clinical Trial Summary

The objectives of the Post Market Surveillance (PMS) study are to evaluate the treatment effect of pramipexole on Restless Legs Syndrome (RLS) severity as measured by International Restless Legs Rating Scale and Global Clinical Impression - Improvement, to evaluate the time to reaching maintenance dose of pramipexole

Clinical Trial Description

n/a

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00721279
Study type Observational
Source Boehringer Ingelheim
Contact
Status Completed
Phase N/A
Start date September 2007
View Details
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