CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 21 enrolled
Drug / intervention
Buspirone +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02803749
NCT02803749Phase 2Completed

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

University of Rochester·interventional·Posted Jun 17, 2016·Updated Jan 2, 2020

In Brief

A Phase 2 clinical trial evaluating Buspirone and Placebo for Parkinson Disease and Anxiety. Completed, enrolled 21 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedJun 17, 2016
Enrollment StartOct 1, 2016
Primary CompletionJan 1, 2019
Study CompletionJan 25, 2019
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 10.0 years ago

Interventions

Buspironedrug

Placebodrug