Evidence map›Paper›PMID 23644911›Full record

Trial reportPsychopharmacology2013

The effect of intranasal oxytocin treatment on conditioned fear extinction and recall in a healthy human sample.

Dean Acheson, David Feifel, Sofieke de Wilde, Rebecca McKinney, James Lohr, Victoria Risbrough

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03376139 (Zonisamide as a New Treatment for Post-Traumatic Stress Disorder and Co-Occurring Alcohol Use Disorder), which is not on this map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
20.7field-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.

NCT03376139 phase2withdrawnnot on this mapstarted 2019, after this paper: background citation

Zonisamide as a New Treatment for Post-Traumatic Stress Disorder and Co-Occurring Alcohol Use Disorder

TypeinterventionalSponsorPharmacotherapies for Alcohol and Substance Use Disorders AllianceRan2019 to 2019Enrolled0ConditionsPost Traumatic Stress Disorder, Alcohol Use DisorderArmsZonisamide, Placebo Comparator
3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 137 citations in OpenAlex.

  1. Effects of intranasal oxytocin on fear extinction learning.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Intranasal Oxytocin Administration Dampens Amygdala Reactivity towards Emotional Faces in Male and Female PTSD Patients.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Trial
  9. Intranasal Oxytocin Affects Amygdala Functional Connectivity after Trauma Script-Driven Imagery in Distressed Recently Trauma-Exposed Individuals.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Trial
  10. Trial
  11. Trial
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

6 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

6 authors at 2 institutions in 2 countries.

Dean AchesonDepartment of Psychiatry, University of California, San Diego, CA, USA.
David Feifel
Sofieke de Wilde
Rebecca McKinney
James Lohr
Victoria Risbrough
University of California, San Diego · USUtrecht University · NL

Funding

1/2-Anti-Psychotic Effects of OxytocinR34MH091285 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FEIFEL, DAVID · 2011 to 2012
$510k
NIMH NIH HHS R34 MH091285NIMH NIH HHS R34MH091285
6 · The paper itself

Abstract

rationaleTo improve outcomes for patients undergoing extinction-based therapies (e.g., exposure therapy) for anxiety disorders such as post-traumatic stress disorder (PTSD), there has been interest in identifying pharmaceutical compounds that might facilitate fear extinction learning and recall. Oxytocin (OT) is a mammalian neuropeptide that modulates activation of fear extinction-based neural circuits and fear responses. Little is known, however, about the effects of OT treatment on conditioned fear responding and extinction in humans.

objectivesThe purpose of the present study was to assess the effects of OT in a fear-potentiated startle task of fear conditioning and extinction.

methodsA double-blind, placebo-controlled study of 44 healthy human participants was conducted. Participants underwent a conditioned fear acquisition procedure, after which they were randomized to treatment group and delivered OT (24 IU) or placebo via intranasal (IN) spray. Forty-five minutes after treatment, participants underwent extinction training. Twenty-four hours later, subjects were tested for extinction recall.

resultsRelative to placebo, the OT group showed increased fear-potentiated startle responding during the earliest stage of extinction training relative to placebo; however, all treatment groups showed the same level of reduced responding by the end of extinction training. Twenty-four hours later, the OT group showed significantly higher recall of extinction relative to placebo.

conclusionsThe current study provides preliminary evidence that OT may facilitate fear extinction recall in humans. These results support further study of OT as a potential adjunctive treatment for extinction-based therapies in fear-related disorders.

Indexed as

AdultConditioning, PsychologicalExtinction, PsychologicalFearFemaleHumansMaleMental RecallOxytocinReflex, StartleTreatment OutcomeYoung AdultOxytocin

Identifiers

PMID23644911
PMCPMC5458114
OpenAlexW2024925365

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.