Status:
COMPLETED
Effect of Ketanserin, Olanzapine, and Lorazepam After LSD Administration on the Acute Response to LSD in Healthy Subjects
Lead Sponsor:
University Hospital, Basel, Switzerland
Conditions:
Healthy
Eligibility:
All Genders
25-65 years
Phase:
PHASE1
Brief Summary
The main objective of this study is to determine whether administration of ketanserin (40 mg), olanzapine (10 mg), and lorazepam (2 mg) after administration of LSD (150 µg) attenuates and shortens the...
Detailed Description
LSD is investigated as treatment for various psychiatric (e.g., depression and anxiety) but also somatic disorders (e.g., cluster headache). In Switzerland, compassionate use of psychedelics including...
Eligibility Criteria
Inclusion
- Age between 25 and 65 years
- Sufficient 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
- Abstaining from xanthine-based liquids and foods from the evenings prior to the study sessions to the end of the study days, limit coffee drinking ≤ 3 cups per day for 7 days prior to study day
- Participants must be willing not to drive a traffic vehicle or to operate machines within 48 h after substance administration
- Willing to use effective contraceptive measures throughout study participation (according to Clinical Trial Facilitation Group (CTFG): Recommendations related to contraception and pregnancy testing in clinical trials)
- Women of childbearing potential must have a negative pregnancy test at the beginning of the study. Pregnancy tests are repeated before each study session.
- Body mass index between 18 - 29 kg/m2
Exclusion
- Chronic or acute medical condition
- Current or previous major psychiatric disorder including psychotic disorder, mania / hypomania, borderline personality disorders.
- Psychotic disorder or bipolar disorder in first-degree relatives
- Known hypersensitivity to LSD, ketanserin, olanzapine or lorazepam
- Hypertension (\>140/90 mmHg) or hypotension (SBP \< 85 mmHg)
- Hallucinogenic substance use (not including cannabis) more than 10 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
- Current substance use disorder (within the last 2 months)
- Tobacco smoking (\>1 cigarette/day)
- Consumption of alcoholic beverages (\>15 drinks/week)
- Not exhibiting consistent startle responding on the screening day (i.e., over 75% discernible responses to six 108 dB 40 ms startle pulses), as this would preclude the ability to measure fear potentiated startle.
- Use of strong CYP2D6 inhibitor
- Use of strong CYP1A2 inhibitor or inducer
Key Trial Info
Start Date :
February 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 30 2025
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT05964647
Start Date
February 1 2024
End Date
June 30 2025
Last Update
November 17 2025
Active Locations (1)
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1
University Hospital Basel
Basel, Canton of Basel-City, Switzerland, 4055