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Clinical Trial Summary

The purpose of this study is to investigate the effects of oral psilocybin in post-traumatic headache. Subjects will be randomized to receive placebo, low dose psilocybin, or high dose psilocybin on two separate test days approximately 14 days apart. Subjects will maintain a headache diary prior to, during, and after the treatments in order to document headache frequency and intensity, as well as associated symptoms. Blood samples will be drawn at various timepoints to measure levels of inflammatory peptides.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03806985
Study type Interventional
Source Yale University
Contact
Status Terminated
Phase Phase 1
Start date March 28, 2019
Completion date June 27, 2023

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