Evidence map›Paper›PMID 27090301›Full record

Trial reportMolecular psychiatry2017

Cocaine self-administration disrupted by the N-methyl-D-aspartate receptor antagonist ketamine: a randomized, crossover trial.

E Dakwar, C L Hart, F R Levin, E V Nunes, R W Foltin

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Molecular psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 99 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  16. Article
  17. Is there a risk of esketamine misuse in clinical practice?Therapeutic advances in drug safety · 2025
    Review
  18. Review
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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

5 authors at 1 institution in 1 country.

E DakwarNew York State Psychiatric Institute, Columbia University College of Physicians and Surgeons, New York, NY, USA.
C L HartNew York State Psychiatric Institute, Columbia University College of Physicians and Surgeons, New York, NY, USA.
F R LevinNew York State Psychiatric Institute, Columbia University College of Physicians and Surgeons, New York, NY, USA.
E V NunesNew York State Psychiatric Institute, Columbia University College of Physicians and Surgeons, New York, NY, USA.
R W FoltinNew York State Psychiatric Institute, Columbia University College of Physicians and Surgeons, New York, NY, USA.
Columbia University · US

Funding

Substance Abuse Treatment Development and Clinical Research MentoringK24DA029647 · NIDA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LEVIN, FRANCES RUDNICK · 2010 to 2019
$1.8M
Brief Potent Glutamatergic Modulation: Applications for Cocaine DependenceK23DA031771 · NIDA · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI DAKWAR, ELIAS · 2011 to 2015
$931k
The Effect of Glutamatergic Modulation on Cocaine Self-AdministrationR21DA035472 · NIDA · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI DAKWAR, ELIAS · 2013 to 2014
$426k
NIDA NIH HHS K23 DA031771NIDA NIH HHS K24 DA029647NIDA NIH HHS R21 DA035472
6 · The paper itself

Abstract

Repeated drug consumption may progress to problematic use by triggering neuroplastic adaptations that attenuate sensitivity to natural rewards while increasing reactivity to craving and drug cues. Converging evidence suggests a single sub-anesthetic dose of the N-methyl-D-aspartate receptor antagonist ketamine may work to correct these neuroadaptations and restore motivation for non-drug rewards. Using an established laboratory model aimed at evaluating behavioral shifts in the salience of cocaine now vs money later, we found that ketamine, as compared to the control, significantly decreased cocaine self-administration by 67% relative to baseline at greater than 24 h post-infusion, the most robust reduction observed to date in human cocaine users and the first to involve mechanisms other than stimulant or dopamine agonist effects. These findings signal new directions in medication development for substance use disorders.

Indexed as

AdultCentral Nervous System StimulantsCocaineCocaine-Related DisordersCravingCross-Over StudiesCuesFemaleHumansKetamineMaleMiddle AgedMotivationReceptors, N-Methyl-D-AspartateSelf AdministrationCentral Nervous System StimulantsCocaineKetamineReceptors, N-Methyl-D-Aspartate

Identifiers

PMID27090301
PMCPMC5435123
OpenAlexW2341144630

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.