A Study to Evaluate the Efficacy and Safety of Cabergoline Compared With Placebo for the Treatment of RLS

PHASE3CompletedINTERVENTIONAL
Enrollment

43

Participants

Timeline

Start Date

November 30, 2002

Study Completion Date

May 31, 2003

Conditions
Restless Legs Syndrome
Interventions
DRUG

Cabergoline

Cabergoline oral tablets administered once daily in the evening: 0.5 mg daily on Days 1 to 3, 1.0 mg daily on Days 4 to 7, 1.5 mg daily on Days 8 to 10, and 2.0 mg daily on Days 11 to 14, followed by a stable dose for an additional 3 weeks

OTHER

Placebo

Placebo oral tablets administered daily for 5 weeks

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY