Effects of MDMA Co-administration on the Response to LSD in Healthy Subjects

Healthy Clinical Trial

— LSD-MDMA  

Official title:

Effects of MDMA Co-administration on the Response to LSD in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04516902
• Other study ID #: BASEC 2020-01829
• Status: Completed
• Phase: Phase 1
• Start date: January 1, 2021
• Est. completion date: August 22, 2022

Study information

• Verified date: August 2022
• Source: University Hospital, Basel, Switzerland
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The acute subjective effects of serotonin (5-HT)2A receptor stimulation with lysergic acid diethylamide (LSD) in humans are mostly positive. However, negative effects such as anxiety, paranoid thinking or loss of trust towards other people are common effects, depending on the dose administered, the personality traits of the person consuming it (set), or the environment in which LSD is taken (setting). Negative psychedelic effects may cause acute distress to the subject and acute anxiety has been linked to less favourable long-term outcomes in patients experimentally treated with LSD or similar substances for the treatment of depression. The 5-HT and oxytocin releaser 3,4-methylenedioxymethamphetamine (MDMA) reliably induces positive mood up to euphoria, comfort, empathy, and feelings of trust. If administered in combination with LSD, MDMA may increase positive subjective drug effects including positive mood, empathy, and trust and reduce negative emotions and anxiety associated with LSD and overall produce a more positive over negative experience. The present study will assess subjective and autonomic effects of LSD alone and in combination with MDMA.

Description:

LSD is a so-called "classic" or serotonergic hallucinogen or psychedelic. Its psychedelic effects are mainly attributed to its potent partial serotonin (5-HT) 5-HT2A receptor agonism. The effects of LSD have been frequently investigated in the past in both healthy participants and patients. Several of these studies described robust and sustained effects of LSD in patients suffering from addiction, anxiety and depression. The acute subjective effects elicited by LSD are mostly positive in humans. However, psychedelic substances like LSD may also cause unpleasant subjective effects like negative thoughts, rumination, anxiety, panic, paranoia, loss of trust towards other people and perceived loss of control, depending on the dose of LSD used, the personality traits of the person consuming it (i.e. 'set'), the environment in which it is consumed (i.e. 'setting'), and other factors yet to be determined. Acute negative psychological effects are considered the main risk of psychedelic substance use in humans. Inducing an overall positive acute response to the psychedelic is critical because several studies showed that a more positive experience is predictive of a greater therapeutic long-term effect of the psychedelic. Therefore, there is a need for methods which are capable of reducing bad drug effects while enhancing good drug effects to optimize a psychedelic experience.

The present study uses 3,4-methylenedioxymethamphetamine (MDMA) as a pharmacological tool to optimize LSD's effects profile by inducing positive mood. MDMA is an amphetamine derivative which, unlike prototypical amphetamines, predominantly enhances serotonergic neurotransmission via release of 5-HT through the serotonin transporter (SERT). Furthermore, MDMA is known to trigger oxytocin release which may contribute to its effects to increase trust, prosociality, and enhanced empathy. The state of well-being induced by MDMA including increased activation and emotional excitation is known to be associated with a better response to psychedelics. Due to its psychological profile, MDMA could be a reliable pharmacological tool to serve as an optimizer of a psychedelic experience by inducing positive emotions.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: August 22, 2022
• Est. primary completion date: August 22, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 25 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Age between 25 and 65 years old

2. Sufficient understanding of the German language

3. Understanding of procedures and risks associated with the study

4. Willing to adhere to the protocol and signing of the consent form

5. Willing to refrain from the consumption of illicit psychoactive substances during the study

6. Abstaining from xanthine-based liquids from the evenings prior to the study sessions and during the sessions

7. Willing not to operate heavy machinery within 48 h of substance administration

8. Willing to use double-barrier birth control throughout study participation

9. Body mass index between 18-29 kg/m2

Exclusion Criteria:

1. Chronic or acute medical condition

2. Current or previous major psychiatric disorder

3. Psychotic disorder or bipolar disorder in first-degree relatives

4. Hypertension (SBP>140/90 mmHg) or hypotension (SBP<85 mmHg)

5. Use of hallucinogenic substances (not including cannabis) more than 20 times or any time within the previous two months

6. Use of MDMA more than 20 times or any time within the previous two months

7. Pregnancy or currently breastfeeding

8. Participation in another clinical trial (currently or within the last 30 days)

9. Use of medication that may interfere with the effects of the study medication

10. Tobacco smoking (>10 cigarettes/day)

11. Consumption of alcoholic beverages (>20 drinks/week)

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• Lysergic Acid Diethylamide
A moderate dose of 100 µg LSD will be administered.
• 3,4-methylenedioxymethamphetamine
A moderate dose of 100 mg MDMA will be administered.

Other:
• LSD Placebo
Pure alcohol instead of an alcoholic solution containing LSD
• MDMA Placebo
Mannitol capsules instead of capsules containing MDMA

Locations

Country	Name	City	State
Switzerland	University Hospital Basel, Clinical Trial Unit	Basel	BS

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Acute subjective effects I	Visual Analog Scales (VAS) assessing the intensity and duration of subjective effects on a scale from 0% - 100% with higher scores representing more intense effects	12 months
Primary	Acute subjective effects II	Adjective Mood Rating Scale (AMRS) assesses the occurrence and intensity of 60 moods on a 4-point Likert scale ranging from "not at all" to "extremely"	12 months
Primary	Acute subjective effects III	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	12 months
Primary	Autonomic effects I	Assessed 18 times on each study day via systolic and diastolic blood pressure	12 months
Primary	Autonomic effects II	Assessed 18 times on each study day via heart rate	12 months
Primary	Autonomic effects III	Assessed 18 times on each study day via tympanic body temperature	12 months
Secondary	Plasma levels of LSD	Assessed 18 times on each study day via blood samples	12 months
Secondary	Plasma levels of MDMA	Assessed 18 times on each study day via blood samples	12 months
Secondary	Plasma levels of blood-derived neurotrophic factor (BDNF)	Assessed 21 times on each study day via blood samples	12 months
Secondary	Plasma levels of oxytocin	Assessed 4 times on each study day via blood samples	12 months
Secondary	Psychological Insight Questionnaire	Assesses the degree of psychological insight caused by a psychedelic experience through 14-items to be answered on a 6-point Likert scale ranging from 0 ("not at all") to 5 ("extremely")	12 months
Secondary	States of Consciousness Questionnaire	Assesses the emergence and intensity of phenomenons occurring in altered states of consciousness on a 6-point Likert scale ranging from 0 ("not at all") to 5 ("extremely")	12 months
Secondary	Spiritual Realms Questionnaire	Assesses the spiritual phenomenons elicited by psychedelic substances through 11 main questions to be answered on a total of 65 sub-ordered 100mm visual analog scales	12 months
Secondary	Effect moderation through personality traits I	Assessed via NEO-Five-Factor-Inventory (NEO-FFI)	Baseline
Secondary	Effect moderation through personality traits II	Assessed via Freiburger Personality Inventory (FPI)	Baseline
Secondary	Effect moderation through personality traits III	Assessed via Saarbrücker Personality Questionnaire (SPF)	Baseline
Secondary	Effect moderation through personality trait IV	Assessed via HEXACO personality inventory	Baseline
Secondary	Effect moderation through personality trait V	Assessed via Defense Style Questionnaire (DSQ-40)	Baseline