Actively Recruiting

Phase 1
Age: 25Years +
All Genders
Healthy Volunteers
NCT06899334

Direct Comparison of Altered States of Consciousness Induced by LSD, Psilocybin, and DMT in Healthy Participants

Led by University Hospital, Basel, Switzerland · Updated on 2025-03-27

24

Participants Needed

1

Research Sites

69 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary objective of this study is to determine whether equivalent moderately high doses of LSD, psilocybin, and DMT produce qualitatively similar peak effects when the effect duration is standardized with ketanserin. A DMT infusion mimicking oral LSD and psilocybin administrations will be tested, as well as intravenously administered ketanserin.

CONDITIONS

Official Title

Direct Comparison of Altered States of Consciousness Induced by LSD, Psilocybin, and DMT in Healthy Participants

Who Can Participate

Age: 25Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Good understanding of the German language
  • Understanding of procedures and risks associated with the study
  • Willing to adhere to the protocol and signing of the consent form
  • Willing to refrain from the consumption of illicit psychoactive substances during the study
  • Willing not to operate heavy machinery within 48 h after administration of a study substance
  • Willing to use effective birth control throughout study participation
  • Body mass index 17 - 34.9 kg/m2
Not Eligible

You will not qualify if you...

  • Relevant chronic or acute medical condition
  • Current or previous major psychiatric disorder (e.g. psychotic disorder)
  • Psychotic disorder or bipolar disorder in first-degree relatives
  • Hypertension (SBP>140/90 mmHg) or hypotension (SBP<85 mmHg)
  • Bradycardia (< 45 bpm)
  • Prolonged QTc interval (males: >450 ms, females: >470 ms)
  • AV block II° (Mobitz type and Webckebach type) and III°
  • Hallucinogenic substance use (not including cannabis) more than 20 times or any time within the previous two months
  • Pregnancy or current breastfeeding
  • Participation in another clinical trial (currently or within the last 30 days)
  • Use of medication that may interfere with the effects of the study medication
  • Tobacco smoking (>10 cigarettes/day)
  • Excessive consumption of alcoholic beverages (>15 drinks/week)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital

Basel, Switzerland, 4056

Actively Recruiting

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Research Team

M

Matthias E Liechti, Prof. Dr. MD

CONTACT

M

Mélusine Humbert-Droz, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

4

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