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Completed

NCT Number: NCT05177419

Effects of LSD on Neuroplasticity in Healthy 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.

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Key information

Conditions

Age range

21 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

University of Fribourg

Fribourg, Canton of Fribourg, 1752, Switzerland

About this study

Neuroplasticity is the brain's ability to reorganize itself and adapt in response to changing environmental conditions or pathological stimuli. Its dysregulation may play a role in the etiology of depression and anxiety disorders, and it is also essential for recovery from neural injury and stroke.

LSD is a potent psychedelic drug and a member of the psychoplastogen family of small molecules, which are able to rapidly stimulate neuroplasticity in cortical neurons following a single dose. Previous research suggests that changes in neuroplasticity may contribute to LSD's long-term effects, which include increases in subjective well-being and life satisfaction, reduced anxiety, and increased openness to experience. Additionally, there is some evidence that LSD and other psychedelics could be viable clinical treatments for depression, anxiety, and addictive disorders, and that changes in neuroplasticity may underlie this clinical potential. However, there is still little direct evidence that LSD or other psychoplastogens enhance cortical plasticity in humans.

The goal of this study is to investigate the effects of LSD on several measures of neuroplasticity in healthy human subjects, as well as other abilities and traits thought to be related to neuroplasticity. Determining whether LSD enhances cortical plasticity, how long this may last, where in the brain it occurs, and what it means for cognition and emotion is essential for understanding LSD's long-term effects, including but not limited to its clinical potential.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 21-55
  • Body mass index 18-29
  • Right-handed as assessed by the Edinburgh Handedness Inventory (score > 60)
  • Fluent understanding of German
  • Willingness to adhere to study protocol
  • Willingness to refrain from taking illicit psychoactive substances for the duration of the study
  • Willingness to refrain from consuming alcohol for 24 hours before each study appointment.
  • Willingness to not operate a motor vehicle or other heavy machinery 48 hours after each substance administration.
  • 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).
  • 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.
  • A friend or relative must be available to accompany the participant home following LSD appointments.

Exclusion criteria

  • Severe chronic or acute medical condition
  • History of any seizure disorder, stroke, or cardiovascular illness
  • History of severe head trauma resulting in loss of consciousness
  • Personal or family history (first-degree relative) of psychotic disorders
  • Current or previous major neurological or psychiatric disorder within the last 3 years (e.g. major depression, anorexia, substance use disorder),
  • History of medically relevant suicide attempts
  • Current use of psychoactive medications
  • Lifetime use of hallucinogens, dissociatives, or entheogens more than 10 times, or any time within the previous three months
  • Regular (daily or near-daily) use of cannabis, alcohol, nicotine, or illicit substances
  • Pregnant or nursing women
  • Presence of any implanted, metal or electronic devices (e.g. pacemaker)
  • Recent or current participation in another clinical trial

Treatment and study plan

Lysergic Acid Diethylamide

Drug

100 micrograms LSD base

Other names: LSD

Primary outcomes

  1. Change in motor evoked potential amplitude after paired associative stimulation (PAS)

    Time frame: Baseline, 8 hours post-treatment, 1 day post-treatment, 1 week post-treatment

    Assessment of capacity for neuroplastic changes in the motor cortex

Secondary outcomes

  1. Change in auditory event-related potential (ERP) amplitude after tetanic stimulation

    Time frame: Baseline, 8 hours post-treatment, 1 day post-treatment, 1 week post-treatment

    Assessment of capacity for neuroplastic changes in the auditory cortex

  2. Plasma and serum levels of brain-derived neurotrophic factor (BDNF)

    Time frame: Baseline, 8 hours post-treatment, 1 day post-treatment, 1 week post-treatment

    Marker of neuroplasticity

  3. Motor learning ability

    Time frame: 1 day post-treatment

    Speed and accuracy on a motor learning task

Sponsors and collaborators

Lead sponsor

University of Fribourg

Other

Registry information

Official study title

Effects of Lysergic Acid Diethylamide (LSD) on Neuroplasticity in Healthy Human Subjects

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Jan 4, 2022
Registry last updated
Apr 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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