drugset / Trial / NCT04386317

Terazosin Effect on Cardiac Changes in Early Parkinson's Disease

NCT04386317

Phase 2 Active not recruiting 15 enrolled Cedars-Sinai Medical Center
NaSingle-groupOpen-labelTreatment

Summary

Parkinson's disease (PD) is characterized by many non-motor symptoms that occur several years before the diagnosis, in particular idiopathic REM behavior disorder (iRBD), which is associated with autonomic impairment. The purpose of this study is to investigate the effect of treatment with the selective post-synaptic a1-adrenergic blocker terazosin on 123I-MIBG myocardial uptake in a population of subjects with defined pre-motor PD risks (i.e. hyposmia and RBD) and abnormal baseline 123I-MIBG uptake, with or without 123I-Ioflupane uptake abnormality or PD motor symptoms. Scintigraphic changes will be correlated to motor and non-motor severity of PD, measured by validated clinical scales and cardiac autonomic function tests.

Timeline

Start
2020-11-01
Primary completion
2025-12-10
Completion
2026-03-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Terazosin Small molecule 5 mg Oral
Subject Terazosin Small molecule 10 mg Oral