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Role of Dopamine, Serotonin and 5-HT2A Receptors in Emotion Processing

Role of Dopamine, Serotonin and 5-HT2A Receptors in Emotion Processing

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03019822
Acronym
LAM
Enrollment
28
Registered
2017-01-13
Start date
2017-02-01
Completion date
2018-09-04
Last updated
2018-10-15

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

Conditions

Healthy

Brief summary

The study will test the effect of dopamine, serotonin, and direct 5-HT2A receptor stimulation on empathy, mood perception, and amygdala activity to fearful stimuli. In addition, we predict associations between subjective effects/alterations in emotion processing tests and functional imaging (fMRI) activity.

Interventions

DRUGLSD

100ug per os, single dose

DRUGMDMA

125mg per os, single dose

40.3mg per os, single dose

DRUGPlacebo

Capsules containing mannitol looking identical to the other drugs

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age between 25 and 50 years. 2. Sufficient understanding of the German language 3. Subjects understand the procedures and the risks associated with the study. 4. Participants must be willing to adhere to the protocol and sign the consent form. 5. Participants must be willing to refrain from taking illicit psychoactive substances during the study. 6. 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. 7. Participants must be willing not to drive a traffic vehicle or to operate machines within 48 h after substance administration. 8. Women of childbearing potential must have a negative pregnancy test at the beginning of the study. Pregnancy tests are repeated before each study session. Women and men must agree to use an effective form of birth control (double-barrier method). 9. Body mass index 18-29 kg/m2.

Exclusion criteria

1. Chronic or acute medical condition 2. Hypertension (\>140/90 mmHg) or Hypotension (SBP\<85 mmHg) 3. Current or previous major psychiatric disorder 4. Psychotic disorder in first-degree relatives 5. Illicit substance use (with the exception of cannabis) more than 10 times or any time within the previous two months. 6. Pregnant or nursing women. 7. Participation in another clinical trial (currently or within the last 30 days) 8. Use of medications that may interfere with the effects of the study medications (any psychiatric medications). 9. fMRI related criteria including: metal implants (clips from operations, cochlea, large red/yellow tattoos in the neck area) 10. Tobacco smoking (\>10 cigarettes/day) 11. Consumption of alcoholic drinks (\>10/week)

Design outcomes

Primary

MeasureTime frameDescription
Emotional enhancement as determined by fMRI12 hoursEmotional enhancement (empathy, oxytocin, mood perception, fMRI amygdala blood oxygen level-dependent (BOLD) signal reactivity to fearful stimuli)
fMRI brain activity1 hourAssociations between subjective effects/alterations in emotion processing with fMRI amygdala BOLD activity

Secondary

MeasureTime frameDescription
Resting State fMRI1 hourAssociation between emotional enhancement and resting state fMRI neuronal activity
Effect Modulation by personality traits (assessed with questionnaires),12 hoursEffect modulation by personality traits (assessed with questionnaires), baseline amygdala reactivity to fear in the fMRI, and genetic polymorphisms determined by genotyping of each subject
Effect Modulation by amygdala reactivity to fear (assessed in the fMRI)12 hoursEffect modulation by personality traits (assessed with questionnaires), baseline amygdala reactivity to fear in the fMRI, and genetic polymorphisms determined by genotyping of each subject
Effect Modulation by genetic polymorphisms (determined by genotyping of each subject)12 hoursEffect modulation by personality traits (assessed with questionnaires), baseline amygdala reactivity to fear in the fMRI, and genetic polymorphisms determined by genotyping of each subject

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026