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Clinical Trial Summary

Proof of effectiveness of Pascoflair using qantitative measurement of electric brain activity during examination stress in 40 subjects suffering from test anxiety. A double-blind, randomized, placebo-controlled, 2-armed, Phase IV study in parallel design.


Clinical Trial Description

Anxiolytic effects of PASCOFLAIR® shall be tested in subjects suffering from test anxiety after single intake by aid of a newly developed, validated method consisting of a combination of eye tracking (following glances) with neurocode tracking (quantitative EEG with a time resolution of 364 ms). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05049447
Study type Interventional
Source Pascoe Pharmazeutische Praeparate GmbH
Contact
Status Completed
Phase Phase 4
Start date May 2015
Completion date August 2015

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