drugset / Trial / NCT00144300

Ophthalmologic Safety Study of Pramipexole Immediate Release (IR) Versus Ropinirole in Early Parkinson's Disease (PD) Patients

NCT00144300

Phase 4 Completed 246 enrolled Boehringer Ingelheim
RandomizedParallel-groupOpen-labelDiagnostic

Summary

To determine if there is any difference in the presence of retinal deterioration in PD patients treated with pramipexole IR versus ropinirole as monitored by comprehensive ophthalmologic assessments from baseline to the end of study at two years.

Timeline

Start
2005-01
Primary completion
2010-09
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pramipexole Unknown Oral
Comparator Ropinirole Small molecule Oral

Indications