CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 15 target
Drug / intervention
Terazosin therapydrug
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/NCT05109364
NCT05109364Phase 2ActiveMonitorUpdated 4mo ago · Completion was 3mo ago
Slow Enrollment

The Effect of alpha1- Adrenergic Receptor Antagonist Therapy on Cardiac and Striatal Transporter Uptake in Pre-Motor and Symptomatic Parkinson's Disease: A Follow up Study

Cedars-Sinai Medical Center·interventional·Posted Nov 5, 2021·Updated Mar 2, 2026

In Brief

A Phase 2 clinical trial evaluating Terazosin therapy for Symptomatic Parkinson Disease and 2 related conditions. Active but no longer recruiting, targeting 15 participants across 1 site.

Signals

Enrolling slower than its timeline implies

Detailed Summary

The purpose of this study is to investigate the long-term effects of treatment with the selective post-synaptic a1-adrenergic blocker terazosin on serial in a population of subjects with defined pre-motor Parkinson's disease (PD) risks and abnormal imaging exams. Imaging changes will be correlated to the presence and severity of motor and non-motor symptoms of PD, measured by validated clinical scales and cardiac autonomic function tests.

Study Details

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

Timeline

Phase 2ActiveOverdue
20222023202420252026
First PostedNov 5, 2021
Enrollment StartSep 23, 2022
Primary CompletionMar 10, 2026
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 4.7 years ago

Interventions

Terazosin therapydrug

Primary procedures in this study are MIBG scan, DAT scan, NM-MRI, and terazosin titration. Subjects will return for research visits and imaging every six months for three years. The investigators hypothesize that the rate of decline in DAT scan123I-Ioflupane uptake will be slower in subjects who have received the a1- Adrenergic Receptor Antagonist Terazosin, resulting in a decreased clinical conversion rate to parkinsonism.