Parkinson Disease Clinical Trial
This study was designed to evaluate the symptomatic effects or potential disease progression slowing down effect of a kind of Traditional Chinese Medicinal Mixture in Parkinson's disease (PD) patients. The treatment phase includes 12 months period of Traditional Chinese Medicinal Mixture per day or placebo and 1 month wash-out period without herbal medicine and placebo.
The design of the study was a prospective, randomized, multicenter, double-blind
placebo-controlled protocol. The intervention includes Traditional Chinese Medicinal Mixture
tid or matched placebo.
Participating study centers include Neurological University Outpatient Clinics and
Neurological Departments of Community-based Hospitals experienced with PD patients.
The primary outcome measure was the combined Unified Parkinson's Disease Rating Scale
(UPDRS).
The hypothesis of this study was that Traditional Chinese Medicinal Mixture improves the
overall wellbeing of PD patients and thus may leads to an improvement of parkinsonian
symptoms in PD patients.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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