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
| Type | Name | Description |
|---|---|---|
| DRUG | Buspirone | |
| DRUG | Placebo |
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.