drugset / Trial / NCT03218969

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

NCT03218969

RandomizedCrossoverDouble-blindTreatment

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.

Timeline

Start
2017-09-18
Primary completion
2018-09-28
Completion
2018-11-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Ecopipam Small molecule 100 mg Oral