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Trials / Completed

CompletedNCT02803749

Buspirone in Parkinson's Disease

The Tolerability of Buspirone for the Treatment of Anxiety in Parkinson's Disease

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
21 (actual)
Sponsor
University of Rochester · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Anxiety is highly prevalent in Parkinson's disease and negatively impacts quality of life yet it frequently remains untreated and there have been no clinical trials dedicated to evaluating the pharmacological treatment of anxiety in Parkinson's disease. Buspirone is effective for the treatment of generalized anxiety disorder in the general and elderly population. It is not known if it is effective for the treatment of anxiety in Parkinson's disease. This is a single-center, placebo-controlled, double-blind design with participants randomized with a 4:1 allocation ratio to flexible dosage buspirone (maximum dosage 30 mg twice daily) or placebo for 12 weeks.

Conditions

Interventions

TypeNameDescription
DRUGBuspirone
DRUGPlacebo

Timeline

Start date
2016-10-01
Primary completion
2019-01-01
Completion
2019-01-25
First posted
2016-06-17
Last updated
2020-01-02
Results posted
2020-01-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02803749. Inclusion in this directory is not an endorsement.

Buspirone in Parkinson's Disease (NCT02803749) · Clinical Trials Directory