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NCT05383313Fut, nem toboroz2. fázis

Antidepressant effects of psilocybin in pharmaco-resistant depression

Psilocybin versus ketamine – fast acting antidepressant strategies in treatment-resistant depression

Forrás: EU CTIS (euclinicaltrials.eu) · Utoljára frissítve: 2026. júl. 8.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

The primary aim of the study is to verify the rapid antidepressant effect of psilocybin 25 mg in comparison with ketamine 250 mg using the MADRS scale completed 24 hours after a single application of the study medication. We assume that after 24 hours psilocybin 25 mg and ketamine 250 mg will have similar antidepressant effects effect (decrease in depressive symptoms according to the MADRS scale) and at the same time the effect will be more pronounced with both substances compared to the antidepressant ineffective midazolam 5 mg.

Állapot (regiszter)
Fut, nem toboroz
Fázis (regiszter)
2. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
60 (tervezett)
Első benyújtás
2024. okt. 14.
Kezdés
2024. nov. 21.
Fő szponzor
Narodni Ustav Dusevniho Zdravi
Betegségek
Depresszió
NCT-szám
NCT05383313
EU CT-szám
2024-515899-13-00
EudraCT-szám
2018-004480-31

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 2. fázis
  • Tervezett résztvevők: 60
  • 1 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) EU CTIS (euclinicaltrials.eu) regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

Ki nem vehet részt

Szó szerint a(z) EU CTIS (euclinicaltrials.eu) forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.

Korábbi kezelés

  • Metal implants from MR incompatible materials
  • Regular use of medication that could interact with psilocybin (assessed by examining physician)
  • Current use of monoamine oxidase inhibitors (MAOIs). Patients can be included if they will medications with an MAOI effect as part of tapering are completely stopped at least 14 days before V0.
  • Previous experience with psilocybin, hallucinogenic mushrooms or ketamine is possible in maximum 10% of patients. This experience must not be within the last 12 months or within current derpestive episodes.
  • Current medication with antidepressants, antipsychotics or other drugs with a direct antagonist effect on 5-HT2A receptors (e.g. trazodone, mirtazapine, mianserin, risperidone, quetiapine, ketanserin) or interruption of their use less than 7 days before administration of the study medication. Patients can be included, but these drugs must be completely discontinued as part of the tapering for at least 7 days before V0.
  • Electroconvulsive therapy (ECT) in the previous 6 months
  • Repetitive transcranial magnetic stimulation (rTMS) in the previous 4 weeks
  • Current dependence on drugs or alcohol (ICD-10: F17.x) excluding tobacco and excluding abstinence lasting more than 2 years

Más betegség

  • Severe psychiatric comorbidity (axis I MINI, ICD-10 F0.X – F99.X with the exception of F32.1-2 or F33.1-2, the severity of the disease is clinically assessed by the examining physician)
  • Condition after stroke, myocardial infarction in the last 6 months
  • Heart failure
  • Severe respiratory failure or acute respiratory depression
  • History of convulsions
  • Other serious somatic diseases or any other circumstance in which there would be a significant increase of blood pressure posed a serious threat to health (assessed by the examining physician)
  • Allergy to components of medicinal products
  • Intracranial hypertension, pulmonary hypertension, uncorrected arterial hypertension (BP > 150/100 mmHg)

Egyéb

  • Untreated or decompensated hyperthyroidism
  • Glaucoma
  • Pacemaker
  • The current depressive phase is severe with psychotic symptoms (ICD-10: F32.2-3, F33.2-3)
  • Daily use of benzodiazepine anxiolytics greater than the equivalent of 10 mg of diazepam
  • MADRS suicidality score (item 10) > 4
  • Suicide attempt in the last 6 months
  • Duration of current depressive episode for more than 2 years
  • Claustrophobia, inability to undergo MR examination
  • Pregnancy or breastfeeding or plan to become pregnant within the next 3 months

Kiket keres a vizsgálat

  • Men and women over the age of 18
  • Diagnosis of moderate to severe depressive disorder without psychotic symptoms - ICD-10 criteria F32.1-2 or F33.1-2 and MADRS score ≥20
  • The duration of the depressive episode is a minimum of 3 months and a maximum of 2 years
  • treatment-resistant disease defined as: a) Failure of at least 2 and at most 4 adequate treatments (6 weeks of adequate therapeutic doses antidepressants, adequate non-pharmacological procedures, e.g. psychotherapy, neurostimulation treatment, phototherapy, etc.) within the current depressive episode, when using at least 2 antidepressants with a different pharmacological mechanism of action (augmentation is the gate as a second treatment) or in a combination of one pharmacological treatment and 1 non-pharmacological one treatment b) Intolerance of 2 different treatments and 1 adequate treatment or c) Intolerance of 3 different antidepressant treatments.
  • Ability to understand and independently complete all protocol-defined examinations and scales and be present at all study visits
  • Have a secured caregiver who will be able to be in personal contact with the patient 5 times a week
  • Clinical trial participants of childbearing age must agree to use the prescribed methods contraception for the duration of the clinical trial: a) Women - Correct use of a highly reliable contraceptive method, i.e. combined hormonal contraception (in oral, vaginal or transdermal drug form), progestagen hormonal contraceptives associated with inhibition of ovulation (in oral or injectable pharmaceutical form), non-hormonal intrauterine device or intrauterine device releasing hormones, possibly the presence of bilateral tubal occlusion, vasectomy in the partner, or observing sexual abstinence. b) Men – Observing sexual abstinence or using an adequate contraceptive method (i.e. condom) in case of sexual intercourse.

Életkor a regiszterben: 18 év – 64 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: EU CTIS (euclinicaltrials.eu)

Helyszínek (1)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Narodni Ustav Dusevniho ZdraviKlecanyCsehországFut, nem toboroz

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