Psilocybin studies
Explore psilocybin studies by research question and study design. Compare human trials, observational reports, reviews and preprints with source-linked evidence.
Free access · No subscription for research tools or data exports
Understand the different kinds of psilocybin study
Psilocybin studies include randomized human trials, observational reports, studies in healthy volunteers, animal and laboratory experiments, and registered trial plans. They answer different questions. A registered study establishes a research plan; an observational improvement does not by itself establish causation. A positive randomized endpoint still needs interpretation alongside the comparator, follow-up and adverse events.
Human clinical studies
Compare the selected depression and alcohol-use studies by population, treatment setting, primary endpoint and follow-up. Their findings concern the supervised interventions studied, not unrestricted use.
Compare selected findings and limitationsCurrent and recruiting studies
Use exact registry recruitment status to locate ongoing psilocybin clinical studies. Start and completion dates are registry facts; they do not establish efficacy, publication or personal eligibility.
Recruiting psilocybin studiesLaboratory and mechanism studies
Mechanistic and animal experiments can help formulate hypotheses. Their endpoints and populations differ from clinical outcomes, so they should not be presented as direct evidence of treatment effectiveness.
Explore mechanism-related literatureReviews, protocols and preprints
Reviews synthesise existing work, protocols describe planned methods, and preprints have not been peer reviewed. Preserve these distinctions when building an evidence set.
Research reading checklistBrowse indexed psilocybin studies
4859 matching records; first 20 shown. Derived labels aid screening and need verification against the methods. Coverage is broad but not exhaustive.
Research questions with source-linked context
Publication dates, study dates and indexing dates may differ. Clinical trial registrations describe planned methods, while primary reports describe findings. Read the editorial policy for source tracking, corrections and classification limits.