Overview

SWITCH:Restless Legs Patients Switched to Ropinirole From Pramipexole

Status:
Completed
Trial end date:
2010-04-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to determine the equipotent dose of ropinirole and pramipexole for patients switched from pramipexole to ropinirole in patients with moderate to severe primary Restless Legs Syndrome (RLS). The rationale behind Switch is that patients with Restless Legs Syndrome can maintain stable efficacy and tolerability if correctly switched from one dopamine agonist to an equipotent dose of another.
Phase:
Phase 4
Details
Lead Sponsor:
Augusta University
Collaborator:
GlaxoSmithKline
Treatments:
Pramipexole
Ropinirole