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COMPLETED
NCT03218969
PHASE1/PHASE2

Treatment of Restless Leg Syndrome (RLS) Augmentation With Ecopipam, a D1 Specific Antagonist

Sponsor: William Ondo, MD

View on ClinicalTrials.gov

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

Interventions

DRUG

Ecopipam

oral drug in subjection currently experiencing dopamine agonist induced augmentation

DRUG

Placebo

matching placebo

Locations (1)

Houston Methodist Hospital

Houston, Texas, United States