Progressive Supranuclear Palsy Clinical Trial
Official title:
Pilot, Exploratory Study With [F18]-FDDNP-PET for in Vivo Diagnose of Tauopathy in Unclassified Parkinsonism
The PET tracer [F18]-FDDNP has a specific affinity for lesions containing tau protein.
The study consists of two phases:
- In the first (cross-sectional) phase it will be assessed the uptake of [18F]-FDDNP in
10 cases with progressive supranuclear palsy (PSP, a tauopathy) en 10 with multi-system
atrophy (MSA, a non-tauopathy), along with 20 individuals with Unclassifiable
Parkinsonism, as previously defined in a European cohort study.
- In the second (longitudinal) phase it will be prospectively followed the 20
unclassifiable patients (at 6, 12 and 18 months) by means of validated scales and
accepted diagnostic criteria in order to try to correlate their eventual clinical
diagnosis with baseline PET findings. On this basis, we endeavour to estimate the
ability of this technique to detect in vivo underlying tau pathology in subjects
initially unclassifiable on clinical grounds.
We hypothesized that:
1. Patients with clinically definite PSP will present an increased uptake in basal
ganglia, brainstem and cerebellum.
2. Patients with clinically defined MSA will not present specific uptake.
3. Part of unclassifiable patients with parkinsonism will present a pattern of uptake
similar to patients with clinically defined PSP and this part along the clinical
follow-up will be meet clinical criteria for diagnose of PSP
n/a
Intervention Model: Single Group Assignment, Masking: Open Label
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