Compound tracker

Ketamine.

A source-backed research page for trial rows and update notes connected to this compound or investigational product. The page is generated from the Notion tracker and should be read as a living research map, not a medical conclusion.

9 trial rows 4 update rows Latest checked: May 12, 2026 All trials
Claim boundary

Trial registration, company topline, CNPV/rolling-review status, recruitment status, public-dashboard data, or review literature do not equal approval, label, reimbursement, access, safety, or efficacy. Related update rows are shown only when they include visible Last checked text and an explicit Claim boundary.

Backlinks

This page links out to registry/source records, the global trial tracker, the updates feed, and matching wiki dossiers when available.

9
Trial rows
N/A / Not Applicable / Phase 2 / Phase 4
Phases tracked
Active / Completed / Not yet recruiting
Statuses seen
NCT07099534 Phase 2 Not yet recruiting updated May 12, 2026

ketamine / BPD — Phase 2 single-arm registry backfill

Condition
Severe borderline personality disorder
Sponsor / institution
University Hospital, Toulouse
Start date
Sep 1, 2026
Tracker note / source boundary

Last checked: 2026-05-16 20:00 UTC. ClinicalTrials.gov lists NCT07099534 as a not-yet-recruiting Phase 2, single-group/open-label pilot sponsored by University Hospital, Toulouse. Estimated enrollment 38; two IV ketamine 0.5 mg/kg infusions 24 hours apart plus Good Psychiatric Management; primary outcome is BSL-23 symptom-severity change from baseline to Day 9. Claim boundary: registry/watch and psychiatric-ketamine context only; no results, no randomized proof, no FDA approval/label/access/reimbursement claim, no broad safety claim, and not classic-psychedelic efficacy evidence.

NCT07317232 Not Applicable Recruiting updated Jan 5, 2026

Ayahuasca, Esketamine and Premenstrual Symptoms

Condition
Healthy Women Volunteers
Sponsor / institution
University of Sao Paulo
Start date
Dec 20, 2025
Tracker note / source boundary

ClinicalTrials.gov manual verification on 2026-04-17 | Overall status: RECRUITING | Exact phase: Not Applicable | Lead sponsor: University of Sao Paulo | Conditions: Healthy Women Volunteers | Interventions: Ayahuasca; Esketamine

NCT07317219 Not Applicable Recruiting updated Jan 5, 2026

Ayahuasca, Esketamine and Body Image Perception

Condition
Healthy Women Volunteers
Sponsor / institution
University of Sao Paulo
Start date
Dec 20, 2025
Tracker note / source boundary

ClinicalTrials.gov manual verification on 2026-04-17 | Overall status: RECRUITING | Exact phase: Not Applicable | Lead sponsor: University of Sao Paulo | Conditions: Healthy Women Volunteers | Interventions: Ayahuasca; Esketamine

NCT07317206 Phase 2 Recruiting updated Jan 5, 2026

Ayahuasca, Esketamine and PTSD

Condition
Posttraumatic Stress Disorder (PTSD)
Sponsor / institution
University of Sao Paulo
Start date
Dec 20, 2025
Tracker note / source boundary

ClinicalTrials.gov manual verification on 2026-04-17 | Overall status: RECRUITING | Exact phase: Phase 2 | Lead sponsor: University of Sao Paulo | Conditions: Posttraumatic Stress Disorder (PTSD) | Interventions: Ayahuasca; Esketamine

NCT07212946 Phase 2 Completed updated Dec 29, 2025

Ayahuasca and Esketamine for Major Depression

Condition
Major Depression Severe
Sponsor / institution
University of Sao Paulo
Start date
Oct 30, 2022
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: University of Sao Paulo | Official title: Four Doses of Ayahuasca or Esketamine in Major Depressive Disorder: a Double-blind Randomized Trial | Condition: Major Depression Severe | Intervention: Ayahuasca; Esketamine | Study type: Interventional | Comparator intervention also includes esketamine, so this row is tagged to both Ayahuasca and Ketamine.

NCT06668571 Phase 2 Recruiting updated Oct 14, 2025

Intravenous Ketamine for Treatment-Resistant Depression

Condition
Depressive Disorder, Treatment-Resistant, Treatment Resistant Depression (TRD)
Sponsor / institution
Mayo Clinic
Start date
Feb 10, 2025
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: RECRUITING | Exact phase: Phase 2 | Lead sponsor: Mayo Clinic | Conditions: Depressive Disorder, Treatment-Resistant; Treatment Resistant Depression (TRD)

NCT05809609 N/A Recruiting updated May 21, 2024

Glutamate Emotion Memory Study

Condition
Treatment Resistant Depression, Depression, Major Depressive Disorder
Sponsor / institution
University of Oxford
Start date
Jul 1, 2022
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: RECRUITING | Exact phase: Not applicable | Lead sponsor: University of Oxford | Conditions: Treatment Resistant Depression; Depression; Major Depressive Disorder

May 15, 2026 Last checked 2026-05-16 20:00 UTC Publication Research

PMID 41621446 — esketamine + dexmedetomidine PCSL retrospective TRD cohort

Claim boundary.retrospective uncontrolled multimodal clinic-regimen signal only; not randomized proof, not classic psychedelic efficacy evidence, not approval/label/access/reimbursement, not medical advice, and not generalizable safety proof.

Last checked: 2026-05-16 20:00 UTC. PubMed abstract describes a Journal of Affective Disorders retrospective cohort of 233 TRD patients receiving esketamine plus dexmedetomidine patient-controlled sleep (PCSL), with follow-up at 1, 3, and 6 months. Abstract reports HAMD/PSQI decreases and response rates of 62.00%, 59.73%, and 58.49%, with no serious adverse events observed during follow-up. Claim boundary: retrospective uncontrolled multimodal clinic-regimen signal only; not randomized proof, not classic psychedelic efficacy evidence, not approval/label/access/reimbursement, not medical advice, and not generalizable safety proof.

Source/tracker note

PubMed PMID 41621446 / DOI 10.1016/j.jad.2026.121311. Abstract: retrospective inclusion of 233 TRD patients; HAMD and PSQI assessed at 1, 3, and 6 months after first esketamine infusion; PCSL and additional esketamine recorded; HAMD/PSQI scores decreased significantly; response rates 62.00%, 59.73%, 58.49%; no serious adverse events observed during follow-up.

May 15, 2026 Last checked 2026-05-16 UTC Publication Research

PubMed 41616859 real-world intranasal esketamine TRD systematic review/meta-analysis

Claim boundary.observational real-world evidence synthesis only; not new approval, label expansion, reimbursement/access finding, proof of comparative efficacy, or broad safety guarantee. Abstract itself cautions that observational evidence and absence of control groups mean effect sizes should be interpreted with caution.

PubMed PMID 41616859 is a systematic review/meta-analysis of nine observational real-world studies of intranasal esketamine for treatment-resistant depression; abstract reports symptom reduction/remission patterns and pooled adverse-event/dissociation estimates.

Source/tracker note

Last checked 2026-05-16 UTC. Claim boundary: observational real-world evidence synthesis only; not new approval, label expansion, reimbursement/access finding, proof of comparative efficacy, or broad safety guarantee. Abstract itself cautions that observational evidence and absence of control groups mean effect sizes should be interpreted with caution.

May 14, 2026 Last checked 2026-05-16 16:00 UTC Publication Research

PMID 42140321 — ketamine/esketamine TRD symptom-network observational study

Claim boundary.observational clinic/precision-medicine correlate; not psychedelic efficacy evidence, not randomized proof, not approval/access/medical advice.

Last checked: 2026-05-16 16:00 UTC. Journal of Affective Disorders abstract reports a MGH Ketamine Clinic observational/network-analysis study of 447 TRD patients receiving acute-phase IV ketamine or intranasal esketamine. Abstract says pre-treatment symptom-network density was higher in non-responders than responders and frames baseline network density as a potential correlate of ketamine outcomes. Claim boundary: observational clinic/precision-medicine correlate; not psychedelic efficacy evidence, not randomized proof, not approval/access/medical advice.

Source/tracker note

Abstract: “447 patients receiving acute-phase intravenous ketamine or intranasal esketamine at the MGH Ketamine Clinic were included.” “Pre-treatment network density was significantly higher in non-responders ... compared to responders ...” “Pre-treatment network density serves as a potential correlate of treatment outcomes of ketamine for TRD.”

May 1, 2026 Last checked 2026-05-16 16:00 UTC Publication Research

PMID 42134962 — UK ketamine misuse primary-care narrative review

Claim boundary.narrative/public-health signal, not clinical efficacy evidence, not US prevalence, not medical advice, and distinct from regulated ketamine/esketamine treatment contexts.

Last checked: 2026-05-16 16:00 UTC. British Journal of General Practice narrative review/public-health article describes rising UK ketamine misuse among young people; PubMed lists May 2026. Abstract says deaths increased six-fold over the past decade, ketamine is now the fifth most commonly used drug among young people, and urinary/abdominal presentations can mask dependence or ketamine-related harm. Claim boundary: narrative/public-health signal, not clinical efficacy evidence, not US prevalence, not medical advice, and distinct from regulated ketamine/esketamine treatment contexts.

Source/tracker note

Abstract: “Ketamine ... has become one of the fastest growing substances of misuse in the UK, with deaths increasing six-fold over the past decade.” “It is now the fifth most commonly used drug among young people...” “presentations frequently occur under the guise of urinary or abdominal symptoms.”

Depressive Disorder, Treatment-Resistant, Treatment Resistant Depression (TRD)Healthy Women VolunteersMajor Depression SevereMajor Depressive DisorderPosttraumatic Stress Disorder (PTSD)Severe borderline personality disorderTreatment Resistant DepressionTreatment Resistant Depression, Depression, Major Depressive Disorder