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LSD microdosing - a dose finding study

LSD microdosing - a dose finding study - LSD microdosing - a dose finding study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON46425
Enrollment
27
Registered
2018-04-11
Start date
2018-05-30
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

subjective effects, cognitive functioning Performance and mood enhancement in society

Interventions

Placebo and 5, 10, 20 µg of LSD in randomized order.

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Previous experience with a psychedelic drug, but not within the past 3 months. * Proficient knowledge of the English language * Written Informed Consent * Understanding the procedures and the risks associated with the study. * Age between 18 and 40 years * Absence of any major medical condition as determined by medical examination and laboratory analysis * Absence of any major psychological condition as determined by medical examination * Free from psychotropic medication * 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 24 h after substance administration. * Normal weight, body mass index (weight/height2) between 18 and 28 kg/m2

Exclusion criteria

Exclusion criteria: * History of drug addiction (determined by the medical questionnaire, drug questionnaire and medical examination) * Previous experience of serious side effects to psychedelic drugs (anxiety or panic attacks) * Pregnancy or lactation * Hypertension (diastolic > 90 mmHg; systolic > 140 mmHg) * Current or history of psychiatric disorder (determined by the medical questionnaire and medical examination) * Psychotic disorder in first-degree relatives * Any chronic or acute medical condition * History of cardiac dysfunctions (arrhythmia, ischemic heart disease,*) * For women: no use of a reliable contraceptive * Tobacco smoking (>20 per day) * Excessive drinking (>20 alcoholic consumptions per week)

Design outcomes

Primary

MeasureTime frame
The study hypothesis is that higher doses of LSD will be associated with increasingly greater and potentially also qualitatively different subjective effects compared to placebo. An additional study parameter is the change in cognitive performance under the influence of LSD compared to placebo.

Secondary

MeasureTime frame
The secondary objective is to characterize the dose-response relationship in LSD-induced changes in cognitive performance.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)