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Psilocybin Administration With 5-HT1a Blockade (PsilBlock1)

1 maggio 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

18

Fase

  • Prima fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Zarmeen Zahid, PhD
  • Numero di telefono: 667-208-8099
  • Email: zzahid2@jh.edu

Luoghi di studio

    • Maryland
      • Baltimore, Maryland, Stati Uniti, 21224-5010
        • Center for Psychedelics and Consciousness Research
        • Investigatore principale:
          • Sandeep M Nayak, MD
        • Contatto:
          • Zarmeen Zahid, PhD
          • Numero di telefono: 667-208-8099
          • Email: zzahid2@jh.edu
        • Sub-investigatore:
          • Zarmeen Zahid, PhD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Scienza basilare
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore placebo: Psilocybin co-administered with placebo
Psilocybin will be co-administered with microcrystalline cellulose placebo.
Microcrystalline cellulose capsules, identical in appearance to the active treatment, containing no pharmacologically active ingredients, will be administered as an inert placebo comparator.
Altri nomi:
  • Microcrystalline cellulose placebo
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.
Sperimentale: Psilocybin co-administered with pindolol
Psilocybin will be co-administered with 5-HT1A antagonist pindolol.
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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Mystical Experiences Questionnaire
Lasso di tempo: From the first dosing session to the end of the second dosing session, approximately 10 days
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.
From the first dosing session to the end of the second dosing session, approximately 10 days

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in alpha power (Spectral Power)
Lasso di tempo: From the first dosing session to the end of the second dosing session, approximately 10 days
Assess changes in neural measures of drug intensity acutely using EEG, specifically global change in alpha power.
From the first dosing session to the end of the second dosing session, approximately 10 days

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Sandeep M Nayak, MD, Center for Psychedelics and Consciousness Research

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 giugno 2026

Completamento primario (Stimato)

15 giugno 2028

Completamento dello studio (Stimato)

15 giugno 2028

Date di iscrizione allo studio

Primo inviato

27 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

27 aprile 2026

Primo Inserito (Effettivo)

4 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

5 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano 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.

Tipo di informazioni di supporto alla condivisione IPD

  • CODICE_ANALITICO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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