- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07565493
Psilocybin Administration With 5-HT1a Blockade (PsilBlock1)
11 septembre 2026 mis à jour par: Johns Hopkins University
The purpose of this study is to assess the effects of 5-HT1A receptor blockade on the acute subjective effects of psilocybin, as measured through subjective survey measures and acute electroencephalography (EEG).
Further, the investigators will assess the effects of psilocybin on post-acute sleep and dreaming through the use of sleep EEG and sleep and dream diaries.
Aperçu de l'étude
Statut
Recrutement
Les conditions
Intervention / Traitement
Description détaillée
This double-blind, randomized, cross-over study (N = 18) will administer a moderate dose of psilocybin trihydrate (18 mg, equivalent to 15 mg psilocybin anhydrate), with pindolol (30 mg), or placebo to assess the effects of 5-HT1A receptor blockade on the acute subjective effects and the acute neurophysiological effects of psilocybin through the use of self-report measures and acute EEG.
Participants will also complete sleep and dream diaries 10 days prior to and 10 days following each drug administration session as well as wear an at-home sleep EEG device for 5 days prior to and 5 days following each drug session.
This study aims to understand the mechanistic basis of the perceptual changes in the altered state of consciousness induced by psilocybin as well as its effects on post-acute sleep and dreaming.
Type d'étude
Interventionnel
Inscription (Estimé)
18
Phase
- Première phase 1
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Zarmeen Zahid, PhD
- Numéro de téléphone: 667-208-8099
- E-mail: psilblock@jh.edu
Lieux d'étude
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Maryland
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Baltimore, Maryland, États-Unis, 21224-5010
- Recrutement
- Center for Psychedelics and Consciousness Research
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Chercheur principal:
- Sandeep M Nayak, MD
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Sous-enquêteur:
- Zarmeen Zahid, PhD
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Contact:
- Zarmeen Zahid, PhD
- Numéro de téléphone: 667-208-8099
- E-mail: psilblock@jh.edu
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-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
Oui
La description
Inclusion criteria:
- 21 - 60 years old
- Must give written or electronic informed consent
- Must have at least a high-school level of education or equivalent (e.g. GED) and are fluent in English
- Must be healthy and psychologically stable as determined by screening for medical and psychiatric problems via a personal interview, a medical questionnaire, a physical examination, an electrocardiogram (ECG), and routine medical blood and urinalysis laboratory tests
- Must agree not to take any as needed (PRN) medications on the mornings of drug sessions
- Must agree not to take sildenafil (Viagra®), tadalafil, or similar medications within 72 hours of each drug administration.
- Must agree to refrain from using all psychoactive substances within 24 hours or 5 elimination half-lives (whichever is greater) before psilocybin administration. Caffeine is the exception.
- Must have a negative urine toxicology report on the same day as drug dosing.
- Who are female and of child-bearing potential and are sexually active, must agree to use highly effective means of birth control (i.e. implants, injectables, combined oral contraceptives, progestin-containing intrauterine device (IUD) or vasectomized partner) for the duration of this study.
- Who are male and sexually active, must agree to use contraception and refrain from sperm donation within 90 days of completing dosing sessions. Effective methods of contraception are barrier, hormonal, and sterilization methods.
Exclusion Criteria:
- Are currently taking a medication with any significant pharmacokinetic or pharmacodynamic interactions with pindolol (e.g. beta-blockers or other anti-hypertensive medications).
- Have a history of orthostatic hypotension or low blood-pressure.
- Have elevated transaminases (2x the upper limit of normal)
- Have a Child-Pugh score that falls within classes B or C.
- Are pregnant (as indicated by a positive urine pregnancy test assessed at intake and before each drug session) or nursing.
- Have cardiovascular conditions: coronary artery disease, stroke, angina, uncontrolled hypertension, a clinically significant ECG abnormality (e.g. atrial fibrillation, corrected QT interval (QTc) > 450 msec), artificial heart valve, symptomatic valvopathy, history of pulmonary hypertension or transient ischemic attack (TIA) in the past year; systolic blood pressure > 139, diastolic blood pressure > 89
- Have epilepsy or a history of seizures
- Have insulin-dependent diabetes; if taking oral hypoglycemic agent, then no history of hypoglycemia
- Are currently taking on a regular (e.g. daily) basis any medications having a centrally acting serotonergic effect, including monoamine oxidase inhibitors (MAOIs). For individuals who have intermittent or PRN use of such medications, psilocybin sessions will not be conducted until at least five half-lives of the agent have elapsed after the last dose.
- Have a current diagnosis of schizophrenia spectrum disorders
- Have a current diagnosis of bipolar spectrum disorders
- Have a current diagnosis of major depressive disorder or Generalized Anxiety Disorder
- Have a current diagnosis or history of substance induced psychotic disorder
- Have a current DSM-5 moderate or severe alcohol or drug use disorder (excluding caffeine and nicotine)
- Have a first degree relative with bipolar I disorder, or schizophrenia spectrum disorder.
- Have a psychiatric condition judged to be incompatible with establishment of safe exposure to psilocybin.
- Have a BMI ≥ 40
- Report a known history of sleep apnea, symptoms indicative of sleep apnea, or have an Apnea-Hypopnea Index (AHI) > 15, or STOP BANG >5
- Taking prescribed hypnotics or other medications known to alter sleep physiology: i.e., Z-drugs, Benzodiazepines, Orexin Agonists or Antagonist, Beta Blockers.
- Regularly taking over-the-counter sleep aids (inc. melatonin and diphenhydramine) and unwilling to abstain during the study.
- Insomnia Severity Index ≥ 10
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Science basique
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Tripler
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Comparateur placebo: Psilocybin co-administered with placebo
Psilocybin will be co-administered with microcrystalline cellulose placebo.
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Microcrystalline cellulose capsules, identical in appearance to the active treatment, containing no pharmacologically active ingredients, will be administered as an inert placebo comparator.
Autres noms:
Psilocybin is a tryptamine psychedelic with 5-HT2A agonist activity.
The psilocybin-induced altered state of consciousness is characterized by changes in sensory perception, cognition, and induction of mystical-type experiences.
These subjective effects will be assessed in each dosing session.
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Expérimental: Psilocybin co-administered with pindolol
Psilocybin will be co-administered with 5-HT1A antagonist pindolol.
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Psilocybin is a tryptamine psychedelic with 5-HT2A agonist activity.
The psilocybin-induced altered state of consciousness is characterized by changes in sensory perception, cognition, and induction of mystical-type experiences.
These subjective effects will be assessed in each dosing session.
Pindolol is a 5-HT1A antagonist drug that will be used as a pharmacological probe for the mechanism of acute subjective effects in the altered state of consciousness induced by psilocybin.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Mystical Experiences Questionnaire
Délai: From the first dosing session to the end of the second dosing session, approximately 10 days
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Assess changes in intensity of the subjective effects induced by psilocybin with co-administration of a 5-HT1A antagonist, pindolol as measured through the mystical experience questionnaire.
Scores can range from 0-150 with a higher score indicating a more intense mystical-type experience.
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From the first dosing session to the end of the second dosing session, approximately 10 days
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in alpha power (Spectral Power)
Délai: From the first dosing session to the end of the second dosing session, approximately 10 days
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Assess changes in neural measures of drug intensity acutely using EEG, specifically global change in alpha power.
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From the first dosing session to the end of the second dosing session, approximately 10 days
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Sandeep M Nayak, MD, Center for Psychedelics and Consciousness Research
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
12 août 2026
Achèvement primaire (Estimé)
15 juin 2028
Achèvement de l'étude (Estimé)
15 juin 2028
Dates d'inscription aux études
Première soumission
27 avril 2026
Première soumission répondant aux critères de contrôle qualité
27 avril 2026
Première publication (Réel)
4 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
14 septembre 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
11 septembre 2026
Dernière vérification
1 septembre 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Produits chimiques organiques
- Composés hétérocycliques
- Composés hétérocycliques, 2 anneaux
- Composés hétérocycliques, anneau fusionné
- Alcaloïdes
- Amines
- Indoles
- Alcools
- Alcaloïdes indole
- Indolizidines
- Indolizines
- Phénoxypropanolamines
- Propanolamines
- Alcools amino
- Propanols
- Tryptamines
- Psilocybine
- Pindolol
Autres numéros d'identification d'étude
- IRB00478908
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
OUI
Description du régime IPD
De-identified data with no participant information will be shared on an open science platform to allow for independent analysis by other researchers.
Subjective survey data, acute EEG, and sleep EEG data will be shared.
Type d'informations de prise en charge du partage d'IPD
- ANALYTIC_CODE
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .