Evidence map›Paper›PMID 38293803›Full record

Trial reportJournal of psychopharmacology (Oxford, England)2024

Ketamine for treatment-resistant major depressive disorder: Double-blind active-controlled crossover study.

Paul Glue, Shona Neehoff, Ben Beaglehole, Shabah Shadli, Neil McNaughton, Natalie J Hughes-Medlicott

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of psychopharmacology (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
9.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Review
  7. Article
  8. Intramuscular Ketamine Pharmacokinetics in Humans: A Review.European journal of drug metabolism and pharmacokinetics · 2026
    Review
  9. Review
  10. Article
  11. Article
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  13. Article
  14. Article
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  16. From Stress to Synapse: The Neuronal Atrophy Pathway to Mood Dysregulation.International journal of molecular sciences · 2025
    Review
  17. Article
  18. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Paul GlueDepartment of Psychological Medicine, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-7305-2800
Shona NeehoffDepartment of Psychological Medicine, University of Otago, Dunedin, New Zealand.
Ben BeagleholeDepartment of Psychological Medicine, University of Otago, Christchurch, New Zealand.
Shabah ShadliDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Neil McNaughtonDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Natalie J Hughes-MedlicottSchool of Pharmacy, University of Otago, Dunedin, New Zealand.
University of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe N-methyl-D-aspartate antagonist ketamine has rapid onset antidepressant activity in treatment-resistant depression (TRD).

aimsTo evaluate mood rating, safety and tolerability data from patients with TRD treated with ketamine and the psychoactive control fentanyl, as part of a larger study to explore EEG biomarkers associated with mood response.

methodsWe evaluated the efficacy and safety of intramuscular racemic ketamine in 25 patients with TRD, using a double-blind active-controlled randomized crossover design. Ketamine doses were 0.5 and 1 mg/kg, and the psychoactive control was fentanyl 50 mcg, given at weekly intervals. RESULTS/OUTCOMES: Within 1 h of ketamine dosing, patients reported reduced depression and anxiety ratings, which persisted for up to 7 days. A dose-response profile for ketamine was noted for dissociative side effects, adverse events and changes in blood pressure; however, changes in mood ratings were broadly similar for both ketamine doses. Overall, 14/25 patients (56%) were responders (⩾50% reduction at 24 h compared with baseline) for either ketamine dose for the Hospital Anxiety and Depression Scale (HADS), and 18/25 (72%) were responders for the HADS-anxiety scale. After fentanyl, only 1/25 (HADS-depression) and 3/25 (HADS-anxiety) were responders. Ketamine was generally safe and well tolerated in this population.

conclusionsOur findings add to the literature confirming ketamine's activity against depressive and anxiety symptoms in patients with TRD.

Indexed as

Depressive Disorder, Treatment-ResistantKetamineMajor Depressive DisorderAntidepressive AgentsCross-Over StudiesDepressionDouble-Blind MethodFentanylHumansTreatment OutcomeAntidepressive AgentsFentanylKetaminedose–responseKetaminemajor depressive disorder

Identifiers

PMID38293803
PMCPMC10863359
OpenAlexW4391389214

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.