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Buspirone, in Combination With Amantadine, for the Treatment of Levodopa-induced Dyskinesia (BUS-PD)
The primary objective of this study is to evaluate the efficacy of buspirone in combination with amantadine in reducing levodopa-induced dyskinesia (LID) in patients with Parkinson's disease (PD).
Details
| Lead sponsor | Oregon Health and Science University |
|---|---|
| Phase | Phase 1 |
| Status | TERMINATED |
| Enrolment | 6 |
| Start date | 2016-01 |
| Completion | 2021-02-23 |
Conditions
- Parkinson's Disease
- Dyskinesias
- Movement Disorders
Interventions
- Buspirone
- Placebo
Primary outcomes
- Area Under the Curve - Dyskinesia - Forceplate — 6 hour levodopa dose cycle
forceplate measurements of levodopa induced dyskinesia taken every 1/2 hour for 6 hours. - Dyskinesia - UDysRS — up to 6 weeks
UDysRS total score comparison - Adverse Events — up to 6 weeks
Adverse Events Monitoring/Frequency
Countries
United States