RecruitingPhase 1NCT06796361

Role of the Serotonin 2A Receptor in Psilocybin-induced Altered States of Consciousness

Role of the Serotonin 2A Receptor in Psilocybin-induced Altered States of Consciousness (PDR-Study)


Sponsor

University Hospital, Basel, Switzerland

Enrollment

16 participants

Start Date

Apr 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Psilocybin (active compound of "magic mushrooms") is a prototypical psychedelic substance that acts via agonism on serotonin (5-HT) 2A receptors. Psilocybin is rapidly metabolized into its active metabolite psilocin. Psilocybin is currently under investigation as potential treatment for various neuropsychiatric disorders. Psilocybin is also widely used for recreational purposes and as research tool in neuroscience. Besides its current clinical development, a clear characterization of the dose-response relationship of psilocybin is lacking. With the present study the investigators aim to close this knowledge gap by administering low (5mg) to high (40mg) single doses of psilocybin to healthy participants. Besides its agonism on 5-HT2A receptors, psilocin also binds to other receptors and inhibits serotonin transporters (SERT). To this data only few studies have investigated these effects and never at a high dose.


Eligibility

Min Age: 25 YearsMax Age: 75 Years

Inclusion Criteria7

  • Age between 25 and 75 years.
  • Sufficient understanding of the German language.
  • Understanding the procedures and the risks that are associated with the study.
  • Participants must be willing to adhere to the protocol and sign the consent form.
  • Participants must be willing to refrain from taking illicit psychoactive substances during the study (not including cannabis).
  • Participants must be willing not to drive a traffic vehicle or to operate machines within 48 h after substance administration.
  • Women of childbearing potential must be willing to use effective birth-control throughout study participation

Exclusion Criteria12

  • Chronic or acute medical condition, including a history of seizures.
  • Body mass index 18-29.9 kg/m2
  • Current or previous major psychiatric disorder (e.g. psychotic disorders, mania / hypomania, anxiety disorders).
  • Psychotic or bipolar disorder in first-degree relatives, not including psychotic disorders secondary to an apparent medical reason, e.g., brain injury, dementia, or lesions of the brain.
  • Hypertension (SBP>140/90 mmHg) or hypotension (SBP<85 mmHg)
  • Psychedelic substance use (with the exception of cannabis) more than 20 times or any time within the previous two months
  • Pregnant or nursing women.
  • Participation in another clinical trial (currently or within the last 30 days).
  • Use of medications that may interfere with the effects of the study medications (any psychiatric medications and any medication with known to interact with the study substances).
  • Tobacco smoking (>10 cigarettes/day).
  • Consumption of alcoholic drinks (>15 drinks / week).
  • Body weight < 45 kg.

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Interventions

DRUGKetanserin 40mg plus Psilocybin 40mg

40mg Ketanserin oral will be administered followed by 40mg Psilocybin.

DRUG40mg Psilocybin

Placebo oral followed by 40mg Psilocybin one hour later.

DRUG20mg Psilocybin

Placebo oral followed by 20mg Psilocybin one hour later.

DRUG10mg Psilocybin

Placebo oral followed by 10mg Psilocybin oral one hour later.

DRUG5mg Psilocybin

Placebo oral followed by 5mg Psilocybin one hour later

OTHERPlacebo

Oral Placebo followed by oral Placebo one hour later


Locations(1)

Clinical Trial Unit

Basel, Canton of Basel-City, Switzerland

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NCT06796361


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