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Clinical Trial Summary

In previous clinical trial work, the investigators observed lasting reductions in headache burden after limited dosing of psilocybin. This purpose of this study is to examine potential sources for this observed effect. This study will measure brain resting state functional connectivity (fMRI), central synaptic density (SV2A PET), peripheral markers of inflammation, circadian rhythm (actigraphy), and sleep (sleep EEG) in both migraine and healthy control participants before and one week after the administration of psilocybin or an active control agent.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06464367
Study type Interventional
Source Yale University
Contact Heather Garrett, BS
Phone 203-937-5711
Email heather.garrett@yale.edu
Status Not yet recruiting
Phase Early Phase 1
Start date September 1, 2024
Completion date December 31, 2026

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