Role of the Serotonin 5-HT2A Receptor in LSD-induced Altered States of Consciousness (LDR-Study)
- Registration Number
- NCT03321136
- Lead Sponsor
- University Hospital, Basel, Switzerland
- Brief Summary
Serotonin receptors, especially the 5HT2A receptor, are thought to be involved in the effects of various recreationally used psychedelic substances such as LSD. LSD potently stimulates the 5-HT2A receptor but also 5-HT2B/C, 5-HT1 and dopaminergic receptors. LSD induces acute transient alterations in waking consciousness including visual perceptual alterations, audio-visual synesthesia, derealization and depersonalization. LSD has therefore been used as experimental tool ("psychotomimetic") in modern psychiatric research to study psychotic-like states and model psychosis in healthy subjects \[1-5\]. However, the dose-effects of 5-HT2A receptor stimulation by LSD has not yet been studied. Additionally, there is still very limited data to what extent the 5HT2A receptor contributes to LSD's effects and its role in the mediation of the full response to LSD at a high dose is unclear. A recent experimental human study showed the 5-HT2A receptor antagonist ketanserin fully blocked the subjective effects of a moderate dose of 100 µg of LSD \[6\]. But, whether the effects of a high 200 µg oral dose of LSD can be blocked by the selective pharmacological 5-HT2A antagonist ketanserin remains to be tested to confirm the critical role of the 5-HT2A receptor in more pronounced alterations of consciousness and perception. The present study therefore explores the role the 5-HT2A receptor in LSD-induced altered states of consciousness using escalating doses of LSD and the 5-HT2A receptor blocker ketanserin administered before a high dose of LSD.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 16
- Age between 25 and 65 years.
- Understanding of the German language.
- Understanding the procedures and the risks 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.
- 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.
- 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 have a negative pregnancy test at the beginning of the study. Pregnancy tests are repeated before each study session.
- Women of childbearing potential must be willing to use double-barrier birth control
- Body mass index 18-29 kg/m2.
- Chronic or acute medical condition
- Current or previous major psychiatric disorder
- Psychotic disorder in first-degree relatives
- Illicit substance use (with the exception of cannabis) more than 10 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)
- Tobacco smoking (>10 cigarettes/day)
- Consumption of alcoholic drinks (>10/week)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description LSD-200, LSD-200-Ketanserin, Placebo, LSD-25, LSD-50, LSD-100 Placebo Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase Placebo, LSD-25, LSD-50, LSD-100, LSD-200, LSD-200-Ketanserin Placebo Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-25, LSD-50, LSD-100, LSD-200, LSD-200-Ketanserin, Placebo Placebo Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-25, LSD-50, LSD-100, LSD-200, LSD-200-Ketanserin, Placebo LSD Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-50, LSD-100, LSD-200, LSD-200-Ketanserin, Placebo, LSD-25 Placebo Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-100, LSD-200, LSD-200-Ketanserin, Placebo, LSD-25, LSD-50 Placebo Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-200, LSD-200-Ketanserin, Placebo, LSD-25, LSD-50, LSD-100 LSD Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-200-Ketanserin, Placebo, LSD-25, LSD-50, LSD-100, LSD-200 Placebo Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase Placebo, LSD-25, LSD-50, LSD-100, LSD-200, LSD-200-Ketanserin LSD Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-50, LSD-100, LSD-200, LSD-200-Ketanserin, Placebo, LSD-25 LSD Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-200-Ketanserin, Placebo, LSD-25, LSD-50, LSD-100, LSD-200 LSD Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase LSD-100, LSD-200, LSD-200-Ketanserin, Placebo, LSD-25, LSD-50 LSD Cross-over within-subjects design with all treatment conditions, separated by a wash-out phase
- Primary Outcome Measures
Name Time Method Altered states of consciousness 18 months total 5D-ASC score (5-Dimensional Altered States of Consciousness Rating Scale)
- Secondary Outcome Measures
Name Time Method Subjective effects 18 months AMRS scales (Adjective mood rating scale)
Psychotomimetic effects 18 months ESI scale (Eppendorf Schizophrenia Inventory)
Mystical-type experiences 18 months SCQ scales (States of consciousness questionnaire)
Autonomic effects 18 months Body temperature
Trial Locations
- Locations (1)
University Hospital
🇨🇭Basel, Switzerland
University Hospital🇨🇭Basel, Switzerland