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Intravenous Plasma Treatment for Parkinson's Disease — yFFP  

Idiopathic Parkinson Disease Clinical Trial

Official title:
Intravenous Young Fresh Frozen Plasma (yFFP) Investigational Treatment for Parkinson's Disease

Clinical Trial Summary

This study will do a preliminary evaluation of a possible treatment for mild-to-moderate Parkinson's disease. Patients will be treated with either transfusions of plasma from young donors. or with placebo transfusions. In the following several months, Parkinson's symptoms will be monitored and compared for the two groups.

Clinical Trial Description

This is a double-blind placebo controlled trial, designed to evaluate the efficacy of plasma from volunteer donors of ages 18-25. This young fresh frozen plasma (yFFP) will be given intravenously in two doses of 12.5 ml/kg each, with 40-56 hours between doses. In the following 24 weeks, Parkinson's symptoms will be monitored using the short version of the Stanford Presenteeism Scale (SPS-6), and a modified version of the UPDRS scale. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04202757
Study type Interventional
Source The Neurology Center
Contact
Status Completed
Phase Early Phase 1
Start date September 14, 2018
Completion date August 8, 2019
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