Image

The Neurobiological Effect of 5-HT2AR Modulation

Recruiting
18 years of age
Both
Phase 1

Powered by AI

Overview

The investigators wish to investigate neurobiological effects of serotonin 2A receptor modulation in healthy volunteers, contrasting effects of an agonist (psilocybin) and an antagonist (ketanserin). Magnetic resonance imaging (MRI) and positron emission tomography (PET) will be used as neuroimaging tools.

Description

This project applies an experimental medicine strategy coupled with human functional and molecular neuroimaging to elucidate the effects of 5-HT2A receptor (5-HT2AR) modulation on brain function and mood in healthy individuals. We compare psilocybin (5-HT2AR agonist) and ketanserin (5-HT2AR antagonist) effects on brain function to identify neural mechanisms mediating the clinical effects of psilocybin and, more broadly, to establish this comparative strategy as a pathway for delineating pharmacological effects on the brain in humans.

Eligibility

Inclusion Criteria:

  1. Healthy individuals above 18 years of age.

Exclusion Criteria (For Subprojects 1, 2a, 2b, and 3):

  1. Presence of or previous primary psychiatric disease (DSM axis 1 or WHO ICD-10 diagnostic classifications) or in first-degree relatives.
  2. Previous or present neurological condition/disease, significant somatic condition/disease or intake of drugs suspected to influence test results.
  3. Non-fluent Danish language skills.
  4. Vision or hearing impairment.
  5. Previous or present learning disability.
  6. Pregnancy.
  7. Breastfeeding.
  8. Contraindications in regard to MRI scanning.
  9. Alcohol or drug abuse.
  10. Allergy to test drugs.
  11. Participation in studies in which participant has received more than 10 mSv of radiation or other significant exposure to radiation.
  12. Abnormal ECG or intake of QT prolonging medication.
  13. Previous significant side-effects in regard to hallucinogenic drugs.
  14. Use of hallucinogenic drugs 6 months previous to inclusion.
  15. Blood donation 3 months before and after project participation
  16. Body weight under 50 kg.
  17. Plasma ferritin levels outside normal range

Exclusion Criteria (For Subproject 2c):

  1. Presence of or previous primary psychiatric disease (DSM IV axis 1 or WHO ICD-10 diagnostic classifications).
  2. Presence of or previous primary psychiatric disease with psychosis symptoms or hypomania (DSM IV axis 1 [drug/alcohol abuse/dependence, schizophrenia and other psychoses] or WHO ICD-10 diagnostic classifications [F10-29, as well as F30-39 with psychotic symptoms, F60]) in first-degree relatives (parents or siblings).
  3. Previous or present neurological condition/disease, significant somatic condition/disease or intake of drugs suspected to influence test results.
  4. Non-fluent Danish language skills or pronounced vision or hearing impairment.
  5. Previous or present learning disability.
  6. Pregnancy.
  7. Breastfeeding.
  8. Contraindications in regard to MRI scanning.
  9. Alcohol or drug abuse.
  10. Allergy to test drugs.
  11. Abnormal ECG or intake of QT prolonging medication.
  12. Previous significant side-effects in regard to hallucinogenic drugs.
  13. Previous use of hallucinogenic drugs.
  14. Body weight under 45 kg.
  15. Ethical concerns regarding the administration of a psychedelic drug.

Study details

Basic Science

NCT03289949

Gitte Moos Knudsen

27 January 2024

Step 1 Get in touch with the nearest study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.