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Direct Comparison of Altered States of Consciousness Induced by LSD and Psilocybin (LSD-psilo)

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University Hospital Basel

Status and phase

Completed
Early Phase 1

Conditions

Healthy

Treatments

Drug: LSD
Drug: Psilocybin

Study type

Interventional

Funder types

Other

Identifiers

NCT03604744
BASEC 2018-00985

Details and patient eligibility

About

LSD (lysergic acid diethylamide) and psilocybin (the active substance in "magic mushrooms") are widely used for recreational purposes. Both substances are also increasingly used in psychiatric and psychological research to induce and investigate alterations in waking consciousness and associated brain functions (functional brain imaging, "model psychosis") . However, it has never been studied whether there are differences in the alterations in mind produced by these two substances. Both LSD and psilocybin are thought to induce hallucinations primarily via stimulation of the 5-HT2A receptor. However, there are differences in the receptor activation profiles between the two substances that may also induce different subjective effects. LSD potently stimulates the 5-HT2A receptor but also 5-HT2B/C, 5-HT1 and D1-3 receptors . Psilocin (the active metabolite of the prodrug psilocybin) also stimulates the 5-HT2A receptor but additionally inhibits the 5-HT transporter. In contrast to LSD, psilocybin has no affinity for D2 receptors. Both substances are used in neuroscience as pharmacological tools. However, there are no modern studies comparing these two substances directly within the same clinical study and research subjects and using validated psychometric tools. Therefore, the investigators will compare the acute effects of LSD, psilocybin and placebo.

Enrollment

28 patients

Sex

All

Ages

25 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age between 25 and 65 years.
  2. Understanding of the German language.
  3. Understanding the procedures and the risks that are associated with the study.
  4. Participants must be willing to adhere to the protocol and sign the consent form.
  5. Participants must be willing to refrain from taking illicit psychoactive substances during the study.
  6. Participants must be willing to drink only alcohol-free liquids and no coffee, black or green tea, or energy drink after midnight of the evening before the study session, as well as during the study day.
  7. Participants must be willing not to drive a traffic vehicle or to operate machines within 48 h after substance administration.
  8. Women of childbearing potential must have a negative pregnancy test at the beginning of the study. Pregnancy tests are repeated before each study session.
  9. Women of childbearing potential must be willing to use double-barrier birth control
  10. Body mass index 18-29 kg/m2.

Exclusion criteria

  1. Chronic or acute medical condition
  2. Current or previous major psychiatric disorder
  3. Psychotic disorder in first-degree relatives
  4. Illicit substance use (with the exception of cannabis) more than 10 times or any time within the previous two months.
  5. Pregnant or nursing women.
  6. Participation in another clinical trial (currently or within the last 30 days)
  7. Use of medications that may interfere with the effects of the study medications (any psychiatric medications)
  8. Tobacco smoking (>10 cigarettes/day)
  9. Consumption of alcoholic drinks (>10/week)
  10. Bodyweight < 50 kg

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

28 participants in 5 patient groups, including a placebo group

LSD-100, LSD-200, Psilocybin-15, Psilocybin-30, Placebo
Experimental group
Description:
Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase
Treatment:
Drug: Psilocybin
Drug: LSD
Drug: Psilocybin
Drug: LSD
LSD-200, Psilocybin-15, Psilocybin-30, Placebo, LSD-100
Placebo Comparator group
Description:
Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase
Treatment:
Drug: Psilocybin
Drug: LSD
Drug: Psilocybin
Drug: LSD
Psilocybin-15, Psilocybin-30, Placebo, LSD-100, LSD-200
Placebo Comparator group
Description:
Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase
Treatment:
Drug: Psilocybin
Drug: LSD
Drug: Psilocybin
Drug: LSD
Psilocybin-30, Placebo, LSD-100, LSD-200, Psilocybin-15
Placebo Comparator group
Description:
Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase
Treatment:
Drug: Psilocybin
Drug: LSD
Drug: Psilocybin
Drug: LSD
Placebo, LSD-100, LSD-200, Psilocybin-15, Psilocybin-30
Placebo Comparator group
Description:
Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase
Treatment:
Drug: Psilocybin
Drug: LSD
Drug: Psilocybin
Drug: LSD

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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