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NCT Number: NCT06899334

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

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.

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Key information

Conditions

Age range

25 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

University Hospital

Basel, 4056, Switzerland

Location status: Recruiting

Location contact

Matthias E Liechti, Prof. Dr. MD

CONTACT

[email protected]

61 328 68 68 ext. +41

Matthias E Liechti, Prof. Dr. MD

PRINCIPAL_INVESTIGATOR

Mélusine Humbert-Droz, MSc

CONTACT

[email protected]

61 328 48 19 ext. +41

About this study

Lysergic acid diethylamide (LSD), psilocybin, and N,N-dimethyltryptamine (DMT) are serotonergic hallucinogens (psychedelics) and currently investigated as therapeutic tools for the treatment of various psychiatric disorders. They are usually administered in a dose range which induces an alteration of consciousness via the stimulation of the serotonin (5-HT)2A receptor. However, there are differences in the receptor activation profiles between the three substances that may induce different subjective effects. Moreover, they exhibit different pharmacokinetic qualities. In comparative studies of LSD and psilocybin blinding was impaired by the different duration of subjective effects. This study aims to ensure blinding by ending all experiences at the same time with the 5HT2A antagonist ketanserin. Moreover, no study has yet directly compared DMT to LSD and psilocybin. The DMT infusion will be modeled in accordance with the course of an oral LSD and psilocybin administration. Therefore, the LPD-study compares the acute and subacute effects of LSD, psilocybin, and DMT while standardizing the time course and the duration of action for all substances.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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)

Treatment and study plan

LSD

Drug

A moderate to high oral dose of 150 µg LSD will be administered followed by 20 mg intravenous ketanserin after 3 h

Psilocybin

Drug

A moderate to high oral dose of 30 mg psilocybin will be administered followed by 20 mg intravenous ketanserin after 3 h

DMT

Drug

A moderate to high, dose-escalating, intravenous infusion up to 2 mg/min DMT will be administered followed by 20 mg intravenous ketanserin after 3 h

Placebo

Drug

An oral and an intravenous placebo will be administered followed by 20 mg intravenous ketanserin after 3 h

Primary outcomes

  1. 1. Altered state of consciousness profile (5D-ASC)

    Time frame: 18 months

    5 Dimensions of Altered States of Consciousness (5D-ASC) consisting of 94 items to be rated on a visual analog scale (0-100 mm), with higher values indicating stronger effects.

Secondary outcomes

  1. Subjective effects (VASs)

    Time frame: 18 months

    Visual Analog Scales assessing the intensity and duration of subjective effects on a scale from 0 - 100 percent with higher scores representing more intense effects.

  2. Mystical-type experiences (PES)

    Time frame: 18 months

    This 100-item Psychedelic Experience Questionnaire/Scale (PES100) is rated on a six-point scale (0 indicating "not at all" and 5 indicatin "extremely"). It comprises distractor items as well as subscales which measure mystical-type effects.

  3. Mystical-type experiences (PAE-PS-ext)

    Time frame: 18 months

    This Phenomenological-Autobiographical-Existential Psychedelic Scale extended (PAE-PS-ext) questionnaire rates psychedelic experiences with a focus on phenomenological, autobiographical, and existential psychedelic experiences (scale from 0 - 100 percent with higher scores representing more intense effects).

  4. 3. Emotional breakthrough inventory (EBI+)

    Time frame: 18 months

    This 18-item questionnaire is a visual analog scale (from 0 - 100 percent with higher scores representing more intense effects) assessing emotional breakthrough throughout the study sessions.

  5. Plasma levels of LSD

    Time frame: 18 months

    Assessed 20 times on each study day via blood samples

  6. Plasma levels of psilocybin

    Time frame: 18 months

    Assessed 20 times on each study day via blood samples

  7. Plasma levels of DMT

    Time frame: 18 months

    Assessed 20 times on each study day via blood samples

  8. Plasma levels of ketanserin

    Time frame: 18 months

    Assessed 20 times on each study day via blood samples

  9. Plasma levels of oxytocin

    Time frame: 18 months

    Assessed 2 times on each study day via blood samples

  10. Plasma levels of prolactin

    Time frame: 18 months

    Assessed 2 times on each study day via blood samples

  11. Plasma levels of cortisol

    Time frame: 18 months

    Assessed 2 times on each study day via blood samples

  12. Autonomic effects I

    Time frame: 18 months

    Assessed 16 times on each study day via systolic and diastolic blood pressure

  13. Autonomic effects II

    Time frame: 18 months

    Assessed 16 times on each study day via heart rate

  14. Autonomic effects III

    Time frame: 18 months

    Assessed one time at screening visit and twice on each study day via ECG (QT-time)

  15. Adverse effects (B-LR)

    Time frame: 18 months

    The 2011 revised Beschwerden-Liste (B-LR) consists of a 40-item list covering a wide variety of symptoms and complaints that are answered with a four-point intensity-scoring ranging from 0 indicating "not at all" to 3 indicating "strong."

  16. Adverse effects (SPSI)

    Time frame: 18 months

    The Swiss Psychedelic Side Effects Inventory evaluates side effects associated with psychedelics using a binary "yes or no" approach. Severity is recorded using a three-point intensity scale ranging from 1 indicating "light" to 3 indicating "strong." The impact is recorded using a five-point scale ranging from -2 "very disadvantageous" to +2 "very advantageous." The relation to the drug is recorded using a five-point scale ranging from 0 indicating "unknown" to 4 indicating "certain."

  17. Adverse Events (AE)

    Time frame: 18 months

    Any report of adverse events will be recorded on a AE-Form.

Study contacts

Contact information is provided by the study sponsor or research team.

Matthias E Liechti, Prof. Dr. MD

CONTACT

[email protected]

61 328 68 68 ext. +41

Mélusine Humbert-Droz, MSc

CONTACT

[email protected]

61 328 48 19 ext. +41

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Official study title

Direct Comparison of Altered States of Consciousness Induced by LSD, Psilocybin, and DMT in a Randomized, Placebo-controlled, Cross-over Trial in Healthy Participants (LPD-Study)

Acronym: LPD

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 27, 2025
Registry last updated
Mar 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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