drugset / Trial / NCT03817554

Pramipexole for Restless Leg Syndrome in Peritoneal Dialysis Patients

NCT03817554 ↗

Phase 4 Terminated 21 enrolled Dong Jie
RandomizedParallel-groupTriple-blindTreatment

Summary

A randomized, double-blind controlled Study from a single center to evaluate the effect and safety of pramipexole on peritoneal dialysis patients with restless legs syndrome

Timeline

Start
2019-07-01
Primary completion
2020-08-31
Completion
2020-08-31

Outcome

Outcome not reported

Stopped (Enrollment): “The recruitment of participants in the study was difficulty.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramipexole Unknown 0.125 mg Oral
Subject Pramipexole Unknown 0.25 mg Oral
Subject Pramipexole Unknown 0.5 mg Oral
Subject Pramipexole Unknown 0.75 mg Oral