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NCT06303739Fut, nem toboroz3. fázis

Psilocybin-Assisted Therapy in Treatment-Resistant Depression

Induction Protocol for Psilocybin-Assisted Therapy in Treatment-Resistant Depression (TRD): A Pilot Study

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. máj. 6.

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Rövid összefoglaló (regiszter, angolul)

The goal of this clinical trial is to test how well psilocybin-assisted therapy works in treating people with depression. The main questions this study aims to answer are: * Does psilocybin with assisted therapy help improve symptoms for people with depression? * How long do the effects of this treatment last? Participants will: * Take part in a couple of screening and preparation visits. * Be given psilocybin in one or two treatment sessions. * Attend a series of follow-up sessions over the following year. * Complete forms and surveys to test how their symptoms have changed and what they thought of their experience. Researchers will also compare whether one treatment or two treatments help improve symptoms more for participants.

Állapot (regiszter)
Fut, nem toboroz
Fázis (regiszter)
3. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
20 (tényleges)
Első benyújtás
2024. febr. 27.
Kezdés
2024. ápr. 19.
Elsődleges befejezés
2026. ápr. 9.
Fő szponzor
University of North Carolina, Chapel Hill
Betegségek
Depresszió
NCT-szám
NCT06303739

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 3. fázis
  • Bevont résztvevők: 20
  • 2024. ápr. 19. és az elsődleges befejezés (2026. ápr. 9.) között
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Alcohol or other substance use disorder (except tobacco/nicotine) that has been active within the 6 months prior to enrollment.
  • Within 72 hours of psilocybin administration, use of nicotine, alcohol, or other controlled substances (use related to over-the-counter or prescribed medications may be allowed per the Primary Investigator's discretion).
  • Current use or use within 4 weeks of psilocybin administration of Monoamine oxidase inhibitors (MAOIs), alcohol dehydrogenase inhibitors and antipsychotics (concomitant medications will be allowed per investigator discretion).
  • Current treatment with buproprion greater than 300mg/day.
  • Prior participation in psilocybin-assisted therapy trial and or regular use of hallucinogens
  • Treatment with another investigational drug or other intervention during study period.

Más betegség

  • Family history (first- or second-degree relatives) or diagnosis of bipolar disorder with psychotic features, schizophrenia, schizoaffective disorder, hallucinogen-induced psychosis, anti-social personality disorder, or other psychotic disorder.
  • Borderline personality disorder, defined by DSM-V criteria, that in the judgement of the Investigator is likely to complicate the assessment of clinical response to study treatments or limits the patient's ability to comply with study procedures.
  • Diagnosis of Obsessive-compulsive disorder or post-traumatic stress disorder.
  • Current delirium, dementia, amnestic disorder, or other cognitive disorders.
  • Any current or past medical or neurological illness (including chronic pain syndromes and/or history of cerebrovascular event (excluding migraine)) that, in the opinion of the investigator, may confound the interpretation of study assessments
  • Known allergic reactions to components of psilocybin.
  • Febrile illness in last 3 weeks.

Laborértékek

  • Medically instability at screening, including hepatic, renal, circulatory, cardiac (arrhythmia, uncontrolled hypertension, systolic BP > 140 mmHg or diastolic BP > 90 mmHg, abnormal QTc), pulmonary or CNS (seizure disorder or treatment with antiepileptic drugs) impairment.

Egyéb

  • Recent use (within past 4 weeks) of esketamine, ketamine or classic hallucinogens (psilocybin-containing mushrooms or LSD) or use of psychedelics within the past 6 months or more than 10 times in lifetime.
  • Participants with active suicidal ideation or plan with a Columbia Suicide Severity Rating Scale (C-SSRS) score greater than or equal to 4.
  • Current active self-injurious behavior, requiring medical attention or per investigator discretion.
  • Current pregnancy or lactation.
  • Current use of tramadol.

Kiket keres a vizsgálat

  • Provision of signed and dated informed consent form.
  • Willingness to comply with all study procedures and availability for the study.
  • Diagnostic and Statistical Manual of Mental Disorders 5 (DSM-V) diagnosis of major depressive disorder.
  • Currently experiencing a major depressive episode, lasting at least 3 months
  • Failure to respond or inability to tolerate at least 2 guideline-concordant pharmacological treatments from different pharmacologic classes during the current major depressive episode
  • Good health evidenced by medical history and routine lab tests
  • No central nervous system (CNS) or neurocognitive impairment
  • Ability to take oral medication and to follow to the psilocybin-assisted therapy protocol
  • Identified support person to accompany patient home after dosing
  • Use of effective contraception throughout the study by those with child-bearing potential
  • Use of condoms or other effective contraceptive methods by males with reproductive potential
  • Fully vaccinated and up to date on vaccination against COVID-19, as defined by Center for Disease Control guidelines
  • Following Lifestyle Considerations throughout study (no nicotine containing products in clinical unit, refrain from operating heavy machinery for the duration of treatment day, no more than two servings 8 hours prior to treatment, no psychoactive drugs 72 hours before treatment, refrain from consuming foods that would interfere with drug absorption, minimize interaction with household immunocompromised contacts)

Életkor a regiszterben: 18 év – 70 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

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HelyszínVárosOrszágHelyszín állapota
UNC Chapel Hill Medical CenterChapel HillEgyesült ÁllamokIsmeretlen állapot

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