Clinical Research Facility, King's College Hospital
London, SE5 9RS, United Kingdom
NCT Number: NCT04959253
A single centre clinical trial to evaluate the feasibility, safety and efficacy of psilocybin, given under supportive conditions, in a randomised, blinded design in adult participants with treatment resistant major depressive disorder. The primary objective is to evaluate feasibility by measuring recruitment rates, dropout rates and by estimating the variance of the primary outcome measure (MADRS).
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Notify Me25 year–80 year
All sexes
Interventional
Phase 2
London, SE5 9RS, United Kingdom
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Exclusions for Pre-Existing Medical Conditions
Participants will be excluded if they have a current diagnosis of ≥1 of:
Past diagnosis of ≥1 of:
A package of psychological therapy and a single dosing session of psilocybin.
A package of psychological therapy and a single dosing session of placebo.
Time frame: From opening to closing of trial recruitment period
Recruitment rates to the trial
Time frame: From time of first enrollment until last participant last visit
Dropout rates in the trial
Time frame: 3 weeks from baseline
The variance in the MADRS between groups
Time frame: 3 weeks from baseline
The change in the Montgomery-Asberg Depression Rating Scale total score from the Baseline Visit (V2 - 1 day prior to treatment) to Week 3 after treatment (V6). Higher scores mean worse depression. Lowest score is 0. Highest score is 60.
Time frame: 6 weeks from baseline
The change in the Montgomery-Asberg Depression Rating Scale total score from the Baseline Visit (V2 - 1 day prior to treatment) to Week 3 after treatment (V6). Higher scores mean worse depression. Lowest score is 0. Highest score is 60.
Time frame: At any point from baseline (day 0) visit until 6-week follow-up
Restart antidepressant medication for any reason, restart medication for continuing depressive symptoms or relapse from a previously recovered state (clinical judgement, supported by the QIDS-SR-16). Participants who withdraw from the study will be censored from the time to event analysis.
Time frame: Week 6
Change from baseline in the WSAS at week 6. Higher scores mean worse impairment. Lowest score = 0. Highest score = 40.
Time frame: Week 3
Change from baseline in the QIDS-SR-16 at week 3. Higher scores mean worse depression symptoms. Minimum score = 0. Maximum score = 27.
Time frame: Week 3
Change from baseline in the GAD-7 at week 3. Higher scores mean worse symptoms. Lowest score = 0. Highest score = 21.
King's College London
Other
A Randomised, Placebo Controlled Trial of Psilocybin in Treatment Resistant Depression: A Feasibility Study
Acronym: PsiDeR
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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