Parkinson's Disease Clinical Trial
Official title:
Developing a Novel Imaging Biomarker in the Differential Diagnosis of Parkinson's Disease and Parkinsonism by 18F-DTBZ PET
This study will compare the brain uptake of 18F- DTBZ in 20 patients with PD, 20 patients with MSA, 20 patients with PSP, 20 patients with CBS, and 20 patients with VaP, 20 patients with ET, and 10 patients with DT.
Study duration is expected to be completed in a period of 4 year. This study is a
uncontrolled, open-label, non-randomized, parallel, and cross-sectional study. Total 130
subjects, including 20 patients with PD, 20 patients with MSA, 20 patients with PSP, 20
patients with CBS, 20 patients with VaP, 20 patients with ET, and 10 patients with DT, will
be enrolled.
Each evaluable subject involved in this study must fulfill all the inclusion and exclusion
criteria according the subject grouping, each subject will have 3 visits in this study, as
one screening visit, one imaging visit, and one safety evaluation visit.
Safety measurement will be evaluated by medical history, vital signs, physical examinations,
laboratory examinations and collecting of adverse events.
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