Healthy Clinical Trial
Official title:
Effects of Lysergic Acid Diethylamide (LSD) on Neuroplasticity in Healthy Human Subjects
Neuroplasticity is the brain's ability to reorganize itself and adapt in response to changing environmental conditions or pathological stimuli. LSD is a potent psychedelic drug which has been able to rapidly stimulate neuroplasticity in animal studies. Various authors have speculated that changes in neuroplasticity may contribute to LSD's long-term effects, but there is still little direct evidence that LSD or other psychedelics enhance neuroplasticity in humans. The goal of this study is to investigate the effects of LSD on several measures of neuroplasticity in healthy human subjects.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | December 1, 2024 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years to 55 Years |
Eligibility | Inclusion Criteria: 1. Aged 21-55 2. Body mass index 18-29 3. Right-handed as assessed by the Edinburgh Handedness Inventory (score > 60) 4. Fluent understanding of German 5. Willingness to adhere to study protocol 6. Willingness to refrain from taking illicit psychoactive substances for the duration of the study 7. Willingness to refrain from consuming alcohol for 24 hours before each study appointment. 8. Willingness to not operate a motor vehicle or other heavy machinery 48 hours after each substance administration. 9. Women of childbearing potential must be willing to use effective birth control during the study (e.g. birth control pill; condoms must be combined with a second reliable method). 10. Women of childbearing potential must have a negative pregnancy test at the beginning of the study. Pregnancy tests will be repeated before each treatment day and must remain negative. 11. A friend or relative must be available to accompany the participant home following LSD appointments. Exclusion Criteria: 1. Severe chronic or acute medical condition 2. History of any seizure disorder, stroke, or cardiovascular illness 3. History of severe head trauma resulting in loss of consciousness 4. Personal or family history (first-degree relative) of psychotic disorders 5. Current or previous major neurological or psychiatric disorder within the last 3 years (e.g. major depression, anorexia, substance use disorder), 6. History of medically relevant suicide attempts 7. Current use of psychoactive medications 8. Lifetime use of hallucinogens, dissociatives, or entheogens more than 10 times, or any time within the previous three months 9. Regular (daily or near-daily) use of cannabis, alcohol, nicotine, or illicit substances 10. Pregnant or nursing women 11. Presence of any implanted, metal or electronic devices (e.g. pacemaker) 12. Recent or current participation in another clinical trial |
Country | Name | City | State |
---|---|---|---|
Switzerland | University of Fribourg | Fribourg | FR |
Lead Sponsor | Collaborator |
---|---|
University of Fribourg |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in motor evoked potential amplitude after paired associative stimulation (PAS) | Assessment of capacity for neuroplastic changes in the motor cortex | Baseline, 8 hours post-treatment, 1 day post-treatment, 1 week post-treatment | |
Secondary | Change in auditory event-related potential (ERP) amplitude after tetanic stimulation | Assessment of capacity for neuroplastic changes in the auditory cortex | Baseline, 8 hours post-treatment, 1 day post-treatment, 1 week post-treatment | |
Secondary | Plasma and serum levels of brain-derived neurotrophic factor (BDNF) | Marker of neuroplasticity | Baseline, 8 hours post-treatment, 1 day post-treatment, 1 week post-treatment | |
Secondary | Motor learning ability | Speed and accuracy on a motor learning task | 1 day post-treatment |
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