Overview

Psilocybin for the Treatment of Migraine Headache

Status:
Active, not recruiting
Trial end date:
2021-10-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to investigate the effects of oral psilocybin in migraine headache. Subjects will each receive a dose of placebo and a dose of psilocybin approximately 14 days apart. Subjects will be randomized to the order of treatment and they will be randomized to receive either low or high dose psilocybin. 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. This preliminary study will inform on the basic effects of psilocybin in migraine headache and inform on the design of larger, more definitive studies.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Yale University
Treatments:
Psilocybin
Criteria
Inclusion Criteria:

- Diagnosis of migraine headache per ICHD-3beta criteria

- Typical pattern of migraine attacks with approximately two migraines or more weekly

- Attacks are managed by means involving no more than twice weekly triptan use

- Age 21 to 65

Exclusion Criteria:

- Axis I psychotic disorder (e.g. schizophrenia, bipolar I, depression with psychosis)

- Axis I psychotic disorder in first degree relative

- Unstable medical condition, severe renal, cardiac or hepatic disease, pacemaker, or
serious central nervous system pathology

- Pregnant, breastfeeding, lack of adequate birth control

- History of intolerance to psilocybin, LSD, or related compounds

- Drug or alcohol abuse within the past 3 months (excluding tobacco)

- Urine toxicology positive to drugs of abuse

- Use of vasoconstrictive medications (i.e. sumatriptan, pseudoephedrine, midodrine)
within 5 half-lives of test days

- Use of serotonergic antiemetics (i.e. ondansetron) in the past 2 weeks

- Use of antidepressant medication (i.e. TCA, MAOI, SSRI) in the past 6 weeks

- Use of steroids or certain other immunomodulatory agents (i.e. azathioprine) in the
past 2 weeks