Evidence map›Paper›PMID 24821196›Full record

Trial reportBiological psychiatry2014

A randomized controlled trial of intranasal ketamine in major depressive disorder.

Kyle A B Lapidus, Cara F Levitch, Andrew M Perez, Jess W Brallier, Michael K Parides, Laili Soleimani, Adriana Feder, Dan V Iosifescu, Dennis S Charney, James W Murrough

4 registry-linked trialsOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Biological psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 197 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
197citing papers in PubMed, 13 pooled it
41.2field-weighted citation impact, top 1% 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.

NCT01304147 nacompletednot on this map

Intranasal (IN) Ketamine in Treatment-Resistant Depression (TRD)

TypeinterventionalSponsorJames MurroughRan2011 to 2014Enrolled20ConditionsMajor Depressive DisorderArmsKetamine, placebo
NCT04234776 phase4unknown statusnot on this mapstarted 2018, after this paper: background citation

Intramuscular Ketamine Versus Escitalopram and Aripiprazole in Acute and Maintenance Treatment of Patients With Treatment-resistant Depression

TypeinterventionalSponsorUniversity of Sao PauloRan2018 to 2021Enrolled88ConditionsDepressive DisorderArmsKetamine, Cognition, Suicide risk, Depression thoughts, Quality of life and disability
NCT05019885 phase2recruitingnot on this mapstarted 2022, after this paper: background citation

A Pilot Study to Assess the Efficacy of Subanesthetic Doses of IV Ketamine in the Treatment Drug Resistant Epilepsy

TypeinterventionalSponsorMadeline FieldsRan2022 to 2026Enrolled8ConditionsDrug Resistant Epilepsy, Medically Refractory Epilepsy, Refractory EpilepsyArmsKetamine Hydrochloride
NCT05214417 phase2unknown statusnot on this mapstarted 2022, after this paper: background citation

Conscious Dying/Conscious Living: Ketamine-Assisted Psychotherapy (KAP) for Patients at End of Life-A Pilot Study for Palliative and Hospice Care

TypeinterventionalSponsorThe Ketamine Research FoundationRan2022 to 2024Enrolled120ConditionsIllness TerminalArmsKetamine Injectable Solution, Naturalistic Control
3 · Its place in the literature

Who cites it

197 citing papers in PubMed, 13 syntheses or guidelines pooled it, 476 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Pooled it
  7. Pooled it
  8. Pooled it
  9. Pooled it
  10. Pooled it
  11. Pooled it
  12. Pooled it
  13. Pooled it
  14. Trial
  15. Trial
  16. Intravenous Ketamine for Late-Life Treatment-Resistant Depression: A Pilot Study of Tolerability, Safety, Clinical Benefits, and Effect on Cognition.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2023
    Trial
  17. Trial
  18. Trial
  19. Trial
  20. Trial

137 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 1 country.

Kyle A B LapidusMood and Anxiety Disorders Program, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York; Fishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York.
Cara F LevitchMood and Anxiety Disorders Program, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York.
Andrew M PerezDepartment of Anesthesiology, Icahn School of Medicine at Mount Sinai, New York.
Jess W BrallierDepartment of Anesthesiology, Icahn School of Medicine at Mount Sinai, New York.
Michael K ParidesDepartment of Health Evidence and Policy, Icahn School of Medicine at Mount Sinai, New York.
Laili SoleimaniMood and Anxiety Disorders Program, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York; James J. Peters Veterans Affairs Medical Center, Bronx, New York.
Adriana FederMood and Anxiety Disorders Program, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York.
Dan V IosifescuMood and Anxiety Disorders Program, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York; Fishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York.
Dennis S CharneyMood and Anxiety Disorders Program, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York; Fishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York; Department of Pharmacology and Systems Therapeutics, Icahn School of Medicine at Mount Sinai, New York.
James W MurroughMood and Anxiety Disorders Program, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York; Fishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York. Electronic address: james.murrough@mssm.edu.
Icahn School of Medicine at Mount Sinai · USAllen Institute for Brain Science · US

Funding

Mount Sinai Institutes for Clinical and Translational SciencesUL1TR000067 · NCATS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SAMPSON, HUGH A · 2012 to 2014
$16.5M
Functional MRI Studies of Emotion in Depression and Rapid Antidepressant ResponseK23MH094707 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MURROUGH, JAMES WARREN · 2011 to 2015
$911k
NCATS NIH HHS UL1 TR000067NCATS NIH HHS UL1TR000067NIMH NIH HHS K23 MH094707NIMH NIH HHS K23MH094707
6 · The paper itself

Abstract

backgroundThe N-methyl-D-aspartate glutamate receptor antagonist ketamine, delivered via an intravenous route, has shown rapid antidepressant effects in patients with treatment-resistant depression. The current study was designed to test the safety, tolerability, and efficacy of intranasal ketamine in patients with depression who had failed at least one prior antidepressant trial.

methodsIn a randomized, double-blind, crossover study, 20 patients with major depression were randomly assigned, and 18 completed 2 treatment days with intranasal ketamine hydrochloride (50 mg) or saline solution. The primary efficacy outcome measure was change in depression severity 24 hours after ketamine or placebo, measured using the Montgomery-Åsberg Depression Rating Scale. Secondary outcomes included persistence of benefit, changes in self-reports of depression, changes in anxiety, and proportion of responders. Potential psychotomimetic, dissociative, hemodynamic, and general adverse effects associated with ketamine were also measured.

resultsPatients showed significant improvement in depressive symptoms at 24 hours after ketamine compared to placebo (t = 4.39, p < .001; estimated mean Montgomery-Åsberg Depression Rating Scale score difference of 7.6 ± 3.7; 95% confidence interval, 3.9-11.3). Response criteria were met by 8 of 18 patients (44%) 24 hours after ketamine administration compared with 1 of 18 (6%) after placebo (p = .033). Intranasal ketamine was well tolerated with minimal psychotomimetic or dissociative effects and was not associated with clinically significant changes in hemodynamic parameters.

conclusionsThis study provides the first controlled evidence for the rapid antidepressant effects of intranasal ketamine. Treatment was associated with minimal adverse effects. If replicated, these findings may lead to novel approaches to the pharmacologic treatment of patients with major depression.

Indexed as

Administration, IntranasalAdultAgedAntidepressive AgentsCross-Over StudiesDouble-Blind MethodFemaleFollow-Up StudiesHumansKetamineMajor Depressive DisorderMaleMiddle AgedPsychiatric Status Rating ScalesTime FactorsTreatment OutcomeAntidepressive AgentsKetaminenorketamineAntidepressantdepressionglutamateintranasalketaminetreatment resistant

Identifiers

PMID24821196
PMCPMC4185009
OpenAlexW1996780673

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.