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Treatment of Restless Leg Syndrome (RLS) Augmentation With Ecopipam, a D1 Specific Antagonist
Sponsor: William Ondo, MD
Summary
This is an exploratory, double blinded cross-over study of the D1 antagonist ecopipam treat patients currently having dopamine agonist induced augmentation in restless legs syndrome. Each arm is 6 weeks composed of an unforced titration up to 100mg/day separated by a 2-week wash-out period. Efficacy points will include the IRLS, augmentation scales, sleep scales, clinical impressions and fatigue/mood scales.
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
INTERVENTIONAL
Enrollment
10
Start Date
2017-09-18
Completion Date
2018-11-28
Last Updated
2026-04-27
Healthy Volunteers
No
Conditions
Interventions
Ecopipam
oral drug in subjection currently experiencing dopamine agonist induced augmentation
Placebo
matching placebo
Locations (1)
Houston Methodist Hospital
Houston, Texas, United States