Psychedelic therapy trials recruiting in Europe: the live index (51 recruiting, updated October 2026)

Europe currently has 51 psychedelic and ketamine-family therapy trials recruiting across 20 countries: Psilocybin (26), MDMA (3), Ketamine & esketamine (13), LSD (6), DMT & 5-MeO-DMT (3). A further 13 CTIS trials are authorised but not recruiting yet. Every row below comes from the EU CTIS register or from the ClinicalTrials.gov-checked trial-site cards in our catalog: with phase, country, site and the registry entry to verify against.

Updated · next scheduled verification: November 2026 (monthly cycle of our regulatory monitor) · dataset: JSON / CSV (CC BY 4.0).

Recruiting trials by substance

SubstanceTrials recruitingJump to list
Psilocybin26All 26 trials →
MDMA3All 3 trials →
Ketamine & esketamine13All 13 trials →
LSD6All 6 trials →
DMT & 5-MeO-DMT3All 3 trials →
Ibogaine0none right now: check the registries

Ketamine/esketamine trials in anaesthetic or perioperative indications are deliberately excluded: this index answers the therapy question, not ketamine as an anaesthetic. Trial sites with their own catalog card: all trial sites grouped by country.

Psilocybin trials (26)

TrialPhaseCountryRecruiting sitesRegistry entry
ERPPAD - Efficacy in Relapse Prevention: Psilocybin in Alcohol use disorder with Depressive symptoms (Alcohol use disorder, depressive symptoms)Phase IIIFranceCentre Hospitalier Universitaire De Bordeaux (Pessac Cedex); Centre Hospitalier de la Côte Basque (Bayonne); CHU Besançon (Besançon); CHU de Bordeaux (Bordeaux); CHU Brest (Brest); CH Le Vinatier (Bron); CHU de Nantes (Nantes); CHU de Nîmes (Nîmes); CHU Saint-Etienne (Saint-Priest)CTIS 2025-525069-65-00
A Study of a Deuterated Psilocin Analog (CYB003) in Humans With Major Depressive DisorderPhase IIICzechia, Germany, Greece, Ireland, Poland, United KingdomInstitute of neuropsychiatric Care (INEP) (Prague); Psyon s.r.o. (Prague); A-SHINE s.r.o. (Předměstí); Universitätsklinikum des Saarlandes und Medizinische Fakultät der Universität des Saarlandes (Homburg); Charité Universitaetsmedizin Berlin (Berlin); University Hospital Frankfurt (Frankfurt am Main); Central Institute of Mental Health (Mannheim); Eginitio Hospital (Athens); Attikon University Hospital (Athens); Papageorgiou General Hospital (Thessaloniki); Sheaf House - Tallaght Adult Mental Health Service (Dublin); La Nua Day Hospital Mental Health Centre (Galway); Uniwersytecki Szpital Kliniczny W Białymstoku (Białystok); Promente - Centrum Neurologii i Psychogeriatrii w Bydgoszczy (Bydgoszcz); UCK (Gdańsk); Centrum Badan Klinicznych PI-House Sp. z o.o (Gdańsk); MTZ Clinical Research Powered by Pratia (Warsaw); Department of Pharmacology and Physiology of CNS (Warsaw); Cambridge University Hospital NHS (Cambridge); Clerkenwell Health - Doncaster (Doncaster); NHS Research Scotland (Edinburgh); Queen Elizabeth University Hospital (Glasgow); St Pancras Clinical Research (London); King's College London (London); Clerkenwell Health - Welbeck Street (London); Re:Cognition Health (London); Clerkenwell Health - Baker Street (London); Wolfson Unit - Cumbria, Northumberland, Tyne and Wear NHS Foundation Trust (Newcastle upon Tyne); Ascend Clinical Research (Reading); Sheffield Health and Social Care NHS Foundation Trust (Sheffield)NCT06793397
CAPSI - Cancer related major depression treated with a single dose of psilocybin - a multicenter randomized placebo controlled double blind clinical trial (Major Depressive Disorder, Malignant tumours ICD 10 C00 to C97)Phase IISwedenSahlgrenska University Hospital-Vastra Gotalandsregionen (Goteborg); Uppsala University Hospital (Uppsala); Region Oerebro Laen (Orebro); Region Stockholm – SLSO (Stockholm)CTIS 2023-505532-35-00
Efficacy of psilocybin and trazodone combination in treatment-resistant depression: a randomized controlled proof-of-concept study (PSILOTRAZ) (Treatment-resistant depression)Phase IIFranceGHU St Anne Psychiatrie et Neurosciences (Paris)CTIS 2024-512911-34-00
POSITRON - PsilOcybin with pSychologIcal supporT foR cOcaiNe: a randomised controlled pilot feasibility trial of psilocybin with psychological support for cocaine use disorder (Cocaine addiction)Phase IIIrelandsee registry entryCTIS 2024-515147-32-02
The therapeutic potential of psilocybin in anorexia nervosa in young adults (Anorexia Nervosa)Phase IISwedensee registry entryCTIS 2024-515163-63-00
Soothing Pain After ChEmotherapy: Psilocybin As INtervention (SPACE-PAIN) — a randomized controlled pilot trial (chemotherapy-induced peripheral neuropathy, chronic neuropathic pain)Phase IINetherlandssee registry entryCTIS 2024-516936-93-02
Psilocybin - a strategy of rapid antidepressant response in depression comorbid with cancer,a randomized double-blind study with the possibility of entering open extension (Depressive disorder comorbid with cancer)Phase IICzechiaNarodni Ustav Dusevniho Zdravi (Klecany); Masarykuv Onkologicky Ustav (Brno-Stred)CTIS 2024-517747-31-00
Regression of Atherosclerosis induced by liFe chAnging Experience with psiLocybin (Stable Ischemic Heart Disease)Phase IICzechiasee registry entryCTIS 2024-517902-27-00
Psilocybin-Assisted Therapy for Severe Alcohol Use Disorder: Feasibility, Clinical Efficacy & (Neuro)Cognitive Mechanisms (Severe Alcohol Use Disorder)Phase IIBelgiumsee registry entryCTIS 2024-518061-10-00
A double-blind, randomized, controlled trial on the effect of PEX010 for prolonged grief disorder (Prolonged grief disorder)Phase IISwedensee registry entryCTIS 2024-518218-24-00
Advancing PRecise Interventions for resistant DEpression: rebalancing brain networks and investigating the trajectories of antidepressant effect with psilocybin and personalized neuromodulation (PRIDE) (Treatment Resistant Depression (TRD))Phase IIItalyUniversita' Degli Studi G. D'Annunzio Di Chieti (Chieti Scalo); ASL Roma 5 (Colleferro (RM)); Azienda Ospedaliero Universitaria - Policlinico Riuniti Foggia (Foggia)CTIS 2024-519844-34-03
Psilocybin AsSisted pSychotherapy for the treatmENt of Gambling disordER : a pilot study (Gambling disorder)Phase IIFrancesee registry entryCTIS 2025-522743-18-00
A phase IIa open-label dose-finding study with lead-in phase evaluating the safety, pharmacokinetics, and attenuating effects of trazodone on the consciousness-altering effects of psilocybin in individuals with Treatment-Resistant Depression (Treatment-Resistant Depression)Phase IIItalysee registry entryCTIS 2025-523346-27-00
Cancer Related Major Depression Treated With a Single Dose of PsilocybinPhase IISwedenregion Västra Götaland (Gothenburg); Norra Stockholms Psykiatri (Stockholm); Psykiatriska Kliniken, Akademiska Sjukhuset (Uppsala); Örebro sjukhus (Örebro)NCT06319378
Psilocybin for Hospitalized Patients with Treatment-resistant DepressionPhase IIBelgiumGhent University Hospital (Ghent)NCT06378229
Psilocybin Therapy for Psychological Distress in Palliative PatientsPhase IICzechia, Denmark, Netherlands, PortugalNational Institute of Mental Health (Prague); Bispebjerg Hospital (Copenhagen); University Medical Center Groningen (UMCG) — PsyPal trial site (Groningen); Champalimaud Foundation (Lisbon)NCT06782724
Safety, Therapeutic Potential, and Mechanisms of Two Psilocybin Doses, Administered With Psychological SupportPhase IISwedenPsykiatrikliniken, Baravägen 1 (Lund)NCT07169747
Boosting recovery through excitation of arousal and awareness in comatose patients: Dose finding study (BREA2KTHROUGH DOSEFINDER) (Coma and other disorders of consciousness due to acute traumatic and non-traumatic brain injury)Phase IDenmarksee registry entryCTIS 2023-503617-30-02
The Neurobiological Effect of 5-HT2AR ModulationPhase IDenmarkNeurobiology Research Unit, Rigshospitalet (Copenhagen)NCT03289949
Role of the Serotonin 2A Receptor in Psilocybin-induced Altered States of ConsciousnessPhase ISwitzerlandClinical Trial Unit (Basel)NCT06796361
PsiloIMAGINE: A Psychedelic-augmented Mental Imagery-based Intervention for Young People With Self-harmPhase IUnited KingdomImperial College London (London)NCT06798636
Digital Intervention for Psychedelic Preparation (DIPP): Comparing Meditation and Music-Based ProgramsPhase IUnited KingdomUniversity College London (London)NCT06815653
Direct Comparison of Altered States of Consciousness Induced by LSD, Psilocybin, and DMT in Healthy ParticipanPhase ISwitzerlandClinical Pharmacology & Toxicology, University Hospital Basel (Basel)NCT06899334
Elucidating the Relevance of the Psychedelic Experience to Psilocybin's Anti-Anhedonic EffectsPhase IAustriaMedical University of Vienna, Department of Psychiatry and Psychotherapy, Division of General Psychiatry (Vienna)NCT07490353
The Impact of Psilocybin on Pain in Fibromyalgia Patients—NetherlandsMaastricht University (Maastricht); Leiden University Medical Center (Leiden)NCT06368492

MDMA trials (3)

TrialPhaseCountryRecruiting sitesRegistry entry
High-Intensity Inpatient MDMA-Assisted Psychotherapy for Treatment-Refractory Posttraumatic Stress Disorder: An Open-Label Pilot Study (posttraumatic stress disorder)Phase IINetherlandsArq National Psychotrauma Centre (Diemen)CTIS 2023-508229-28-00
Acute Analgesic Effects of MDMA on Experimentally Induced Acute Pain, Hyperalgesia and Allodynia in Healthy PaPhase ISwitzerlandClinical Pharmacology & Toxicology, University Hospital Basel (Basel)NCT07494214
Plasma Oxytocin Changes in Response to Low-dose MDMA vs. Placebo in Patients With Arginine Vasopressin Deficie—SwitzerlandUniversity Hospital Basel (Basel)NCT06789705

Ketamine & esketamine trials (13)

TrialPhaseCountryRecruiting sitesRegistry entry
MOODBOOSTER« Early efficacy of ketamine compared to placebo, in add-on therapy of venlafaxine for inpatients with severe unipolar major depressive episodes: a double blind randomized controlled trial » (Major depressive disorder with current severe major depressive episode)Phase IIIFranceBicetre Hospital (Le Kremlin Bicetre Cedex); Commissariat A L'energie Atomique Et Aux Energies Alternatives (Orsay Cedex); Etablissement Public De Sante Barthelemy Durand (Etampes Cedex)CTIS 2023-506597-12-00
A randomised, controlled trial to investigate the effect of a six-week intensified pharmacological treatment for major depressive disorder compared to treatment as usual in subjects who had a first-time treatment failure on their first-line treatment. (Major depressive disorder)Phase IIIAustria, Germany, Greece, Italy, SpainLwl-Klinik Dortmund (Dortmund); Universitätsklinik für Psychiatrie und Psychotherapie Bielefeld (Bielefeld); Westfaelische Wilhelms-Universitaet Muenster (Muenster); Azienda Ospedaliera Universitaria Citta' Della Salute E Della Scienza Di Torino (Turin); University Of Brescia (Brescia); Clinica Psichiatrica, 1st floor (Cagliari); Hospital Clinic of Barcelona (Barcelona)CTIS 2023-506617-21-00
The additive effect of ketamine in combination with electroconvulsive stimulation (ECS) in major depressive disorder (MDD): a translational study (Major Depressive Disorder (MDD))Phase IIIItalyOspedale San Raffaele S.r.l. (Milan)CTIS 2024-512559-20-01
Comparison between esketamine nasal spray versus aripiprazole, both in combination with an antidepressant, in the refractory major depression disorder (RMDD) in elderly patients (CESAR) (Refractory major depression disorder (RMDD))Phase IIISpainFundació Hospitalàries Barcelona Nord (Barcelona); Fundació Hospitalàries Sant Boi (Sant Boi De Llobregat); Fundació Hospitalàries Martorell (Barcelona); Fundació Hospitalàries Sant Boi_Granollers (Granollers); Centro Sociosanitario Hermanas Hospitalarias de Palencia (Palencia); Clínica Psiquiátrica Padre Menni (Pamplona); Corporacion Sanitaria Parc Tauli (Sabadell, Barcelona); Hospital Universitario Virgen del Rocio (Sevilla); Vall d'Hebron Hospital (Barcelona); Hospital De La Santa Creu i Sant Pau (Barcelona)CTIS 2024-512672-34-00
A Double-blind, Randomized, Psychoactive Placebo-controlled Study to Evaluate the Efficacy and Safety of Intranasal Esketamine 84 mg in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder in Adolescent Participants with Acute Suicidal Ideation or Behavior (Major Depressive Disorder)Phase IIIHungary, Italy, Romania, Spainsee registry entryCTIS 2024-518615-19-00
Ketamine for the treatment of depressive and negative symptoms in patients with schizophrenia: a randomized controlled cross-over pilot study. (Negative and depressive symptoms in schizophrenia / schizoaffective disorder)Phase IIIAustriasee registry entryCTIS 2024-519097-39-01
Esketamine nasal spray (Spravato) for the treatment of therapy-resistant bipolar depression. An open-label pilot trial. (Bipolar disorder- depressive episode)Phase IINetherlandsAcademisch Ziekenhuis Leiden (Leiden)CTIS 2023-508125-27-00
Pharmacologic treatment augmentation in chronic depression “randomized, controlled, double blinded, phase II study” (Diagnosis of chronic depression)Phase IIGermanyUniversitaetsklinikum Tuebingen AöR (Tuebingen); Universitaetsklinikum Jena KöR (Jena); LMU Klinikum Muenchen AöR (Munich)CTIS 2024-512478-86-00
Ketamine maintenance treatment for depression: A multicenter open-label randomized controlled trial (Major Depression Disorder (MDD))Phase IINorwaysee registry entryCTIS 2025-521330-29-00
Ketamine for combined depression and alcohol use disorder: A blinded randomized active placebo-controlled trial (the KeDA trial) (Depression, Alcohol use disorder)Phase I/IINorwayUniversitetssykehuset Nord-Norge HF (Tromsoe); Østfold Hospital Trust (Grålum)CTIS 2023-506052-24-00
Clinical trial—Austria, ItalyINTENSIFY MDD trial site — University of Cagliari (Cagliari); INTENSIFY MDD trial site — Università degli Studi della Campania Luigi Vanvitelli (Naples); INTENSIFY MDD trial site — AOU Città della Salute e della Scienza di Torino (Turin); INTENSIFY MDD trial site — Medical University Innsbruck (Innsbruck); INTENSIFY MDD trial site — Università degli Studi di Brescia (Brescia)NCT05973851
Clinical trial—CroatiaUniversity of Zagreb School of Medicine (esketamine observational study) (Zagreb)NCT07002684
Clinical trial—HungaryPetz Aladár Egyetemi Oktató Kórház (AVENUE trial) (Győr); Szegedi Tudományegyetem (AVENUE trial) (Szeged)NCT07227454

LSD trials (6)

TrialPhaseCountryRecruiting sitesRegistry entry
Efficacy and safety of minidosing lysergic acid diethylamide (LSD) for chronic cluster headache: a randomized placebo-controlled study (Chronic cluster headache)Phase IINetherlandssee registry entryCTIS 2024-520305-39-00
Lysergic Acid Diethylamide (LSD) as Treatment for Cluster HeadachePhase IISwitzerlandClinical Pharmacology & Toxicology, University Hospital Basel (Basel)NCT03781128
LSD Treatment for Persons With Alcohol Use DisorderPhase IISwitzerlandUniversity Hospital of Psychiatry, University of Basel (Basel); University Hospital of Psychiatry, University of Bern (Bern)NCT05474989
LSD to Improve Cluster Headache Impact TrialPhase IINetherlandsLeiden University Medical Center (LUMC) (Leiden); Canisius-Wilhelmina Ziekenhuis (CWZ) (Nijmegen)NCT05477459
Lysergic Acid Diethylamide (LSD) in Palliative CarePhase IISwitzerlandUniversity Hospital Basel, Division of Clinical Pharmacology and Toxicology (Basel); University Hospital Geneva, Palliative medicine department (Collonge-Bellerive); Spital Uster AG, Division of Internal Medicine (Uster); University Hospital Zurich, Clinic for Radio-Oncology, Competence Centre Palliative Care (Zurich)NCT05883540
Pharmacokinetics of Didehydro-LSD (DDH-LSD) Compared With LSD—SwitzerlandUniversity Hospital Basel (Basel)NCT07309471

DMT & 5-MeO-DMT trials (3)

TrialPhaseCountryRecruiting sitesRegistry entry
Acute Effects of Intravenous 5-MeO-DMT in Healthy ParticipantsPhase ISwitzerlandUniversity Hospital Basel (Basel)NCT07444788
Clinical trial—United KingdomMAC Clinical Research (Liverpool); Hammersmith Medicines Research (London); King's College London, Clinical Trials Facility (London)NCT05660642
Antidepressant Response of DMT Masked With Propofol—SwitzerlandUniversity Hospital Basel (Basel)NCT06927076

How to get into a trial

The route is the same everywhere: find a trial and read its eligibility criteria, contact the site directly (registry listings lag reality), then pre-screening and a site screening visit. Participation is free, voluntary and ethics-committee supervised; you can withdraw at any time without losing your regular care. And: most applicants are screened out, that is the norm, not a judgment. What randomization, placebo and consent mean in practice, the common exclusion criteria and what a dosing day looks like are covered in the full guide: joining a psychedelic clinical trial in Europe. To see whether your profile broadly fits, start with the eligibility check.

Where the data comes from

Two sources, both public: the EU trials register CTIS (euclinicaltrials.eu), from which we pull all psychedelic-substance trials, and our catalog's trial-site cards, whose ClinicalTrials.gov recruiting statuses are refreshed via the official API. Trials listed in both registers are merged. The full index is free to reuse as a dataset (CC BY 4.0, attribution line in the dataset meta): trials-index.json / trials-index.csv. Context in numbers: psychedelic therapy in Europe, statistics; what is changing on the regulatory side: the monthly regulatory monitor.

Frequently asked questions

Which psychedelic therapy trials are recruiting in Europe?

The PsyAccess index currently lists 51 psychedelic and ketamine-family therapy trials recruiting across 20 European countries (updated October 2026): Psilocybin (26), MDMA (3), Ketamine & esketamine (13), LSD (6), DMT & 5-MeO-DMT (3). The full table above gives each trial's phase, country, recruiting sites from our catalog and the registry entry (CTIS or ClinicalTrials.gov). A further 13 CTIS trials are authorised but not recruiting yet.

How do I join a psychedelic clinical trial in Europe?

Three steps: (1) find a trial in this index or in the registries (euclinicaltrials.eu, ClinicalTrials.gov) and read its eligibility criteria; (2) contact the trial site directly, registry listings lag reality; (3) go through pre-screening and a site screening visit. Most applicants are screened out, that is normal and not a judgment on you. Our guide to joining a trial covers the whole funnel.

Do I have to pay to take part in a psychedelic trial?

No. Clinical trial treatment and all study procedures are free of charge, and travel expenses are commonly reimbursed. A legitimate trial never charges participants to join.

How up to date is this index?

The data comes from the EU CTIS register (snapshot October 2026) and from the ClinicalTrials.gov status refresh behind our trial-site cards. The index runs on the same monthly cycle as our regulatory monitor; next scheduled verification: November 2026. Recruiting statuses change fast, always check the linked registry entry before applying.