Evidence map›Paper›PMID 35046508›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2022

Dose-related effects of ketamine for antidepressant-resistant symptoms of posttraumatic stress disorder in veterans and active duty military: a double-blind, randomized, placebo-controlled multi-center clinical trial.

Chadi G Abdallah, John D Roache, Ralitza Gueorguieva, Lynnette A Averill, Stacey Young-McCaughan, Paulo R Shiroma, Prerana Purohit, Antoinette Brundige, William Murff, Kyung-Heup Ahn and 22 more

Erratum issued Registry-linked trialOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02655692 (CAP-Ketamine for Antidepressant Resistant PTSD), which is not on this map. Cited by 65 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 8 pooled it
16.2field-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.

NCT02655692 phase2completednot on this map

CAP-Ketamine for Antidepressant Resistant PTSD

TypeinterventionalSponsorVA Office of Research and DevelopmentRan2016 to 2020Enrolled163ConditionsPTSD, Posttraumatic Stress DisorderArmsKetamine, Placebo/Saline
3 · Its place in the literature

Who cites it

65 citing papers in PubMed, 8 syntheses or guidelines pooled it, 101 citations in OpenAlex.

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  8. Evidence for the beneficial effect of ketamine in the treatment of patients with post-traumatic stress disorder: A systematic review and meta-analysis.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Pooled it
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  10. A pilot randomized controlled trial of ketamine in Borderline Personality Disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Trial
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5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors at 9 institutions in 1 country.

Chadi G AbdallahNational Center for PTSD, Clinical Neurosciences Division, US Department of Veterans Affairs, West Haven, CT, USA. chadi.abdallah@bcm.edu.ORCID http://orcid.org/0000-0001-5783-6181
John D RoacheDepartment of Psychiatry & Behavioral Sciences, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Ralitza GueorguievaDepartment of Biostatistics, School of Public Health, Yale University School of Medicine, New Haven, CT, USA.
Lynnette A AverillNational Center for PTSD, Clinical Neurosciences Division, US Department of Veterans Affairs, West Haven, CT, USA.
Stacey Young-McCaughanDepartment of Psychiatry & Behavioral Sciences, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Paulo R ShiromaMinneapolis VA Medical Center and the Department of Psychiatry University of Minnesota, Minneapolis, MN, USA.
Prerana PurohitNational Center for PTSD, Clinical Neurosciences Division, US Department of Veterans Affairs, West Haven, CT, USA.
Antoinette BrundigeDepartment of Psychiatry & Behavioral Sciences, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
William MurffDepartment of Psychiatry & Behavioral Sciences, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Kyung-Heup AhnDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Mohamed A SherifDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Eric J BaltutisMinneapolis VA Medical Center and the Department of Psychiatry University of Minnesota, Minneapolis, MN, USA.
Mohini RanganathanDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Deepak D'SouzaDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0003-3141-1462
Brenda MartiniNational Center for PTSD, Clinical Neurosciences Division, US Department of Veterans Affairs, West Haven, CT, USA.
Steven M SouthwickNational Center for PTSD, Clinical Neurosciences Division, US Department of Veterans Affairs, West Haven, CT, USA.
Ismene L PetrakisNational Center for PTSD, Clinical Neurosciences Division, US Department of Veterans Affairs, West Haven, CT, USA.
Rebecca R BursonDepartment of Behavioral Health, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Kevin B GuthmillerDepartment of Pain Management, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Argelio L López-RocaDepartment of Behavioral Health, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Karl A LautenschlagerDepartment of Pain Management, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
John P McCallinDepartment of Rehabilitation, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Matthew B HochDepartment of Rehabilitation, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Alexandar TimchenkoDepartment of Rehabilitation, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Sergio E SouzaDepartment of Rehabilitation, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Charles E BryantDepartment of Rehabilitation, Brooke Army Medical Center, Joint Base San Antonio - Fort Sam Houston, Houston, TX, USA.
Jim MintzDepartment of Psychiatry & Behavioral Sciences, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Brett T LitzMassachusetts Veterans Epidemiology Research and Information Center, VA Boston Healthcare System, Boston, MA, USA.
Douglas E WilliamsonDepartment of Psychiatry and Behavioral Sciences, Duke Health, Durham, NC, USA.
Terence M KeaneDepartment of Psychiatry, Boston University School of Medicine, Boston, MA, USA.
Alan L PetersonDepartment of Psychiatry & Behavioral Sciences, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
John H KrystalNational Center for PTSD, Clinical Neurosciences Division, US Department of Veterans Affairs, West Haven, CT, USA.ORCID http://orcid.org/0000-0001-6952-1726
Brooke Army Medical Center · USThe University of Texas Health Science Center at San Antonio · USUnited States Department of Veterans Affairs · USYale University · USBoston University · USMichael E. DeBakey VA Medical Center · USUniversity of Minnesota · USDurham VA Health Care System · USUniversity of Southern California · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Advancing the Research Careers of Women and PEERs in Brain ScienceR25NS124530 · NINDS · BROWN UNIVERSITY · PI CARLOS D AIZENMAN, Diane Lipscombe · 2022 to 2026
$1.3M
NCATS NIH HHS UL1 TR001863NINDS NIH HHS R25 NS124530
6 · The paper itself

Abstract

This study tested the efficacy of repeated intravenous ketamine doses to reduce symptoms of posttraumatic stress disorder (PTSD). Veterans and service members with PTSD (n = 158) who failed previous antidepressant treatment were randomized to 8 infusions administered twice weekly of intravenous placebo (n = 54), low dose (0.2 mg/kg; n = 53) or standard dose (0.5 mg/kg; n = 51) ketamine. Participants were assessed at baseline, during treatment, and for 4 weeks after their last infusion. Primary analyses used mixed effects models. The primary outcome measure was the self-report PTSD Checklist for DSM-5 (PCL-5), and secondary outcome measures were the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) and the Montgomery Åsberg Depression Rating Scale (MADRS). There were no significant group-by-time interactions for PTSD symptoms measured by the PCL-5 or CAPS-5. The standard ketamine dose ameliorated depression measured by the MADRS significantly more than placebo. Ketamine produced dose-related dissociative and psychotomimetic effects, which returned to baseline within 2 h and were less pronounced with repeated administration. There was no evidence of differential treatment discontinuation by ketamine dose, consistent with good tolerability. This clinical trial failed to find a significant dose-related effect of ketamine on PTSD symptoms. Secondary analyses suggested that the standard dose exerted rapid antidepressant effects. Further studies are needed to determine the role of ketamine in PTSD treatment. ClinicalTrials.gov identifier: NCT02655692.

Indexed as

KetamineMilitary PersonnelStress Disorders, Post-TraumaticVeteransAntidepressive AgentsDouble-Blind MethodHumansTreatment OutcomeAntidepressive AgentsKetamine

Identifiers

PMID35046508
PMCPMC8767037
OpenAlexW4226063380

What OpenQuestion holds

Textmetadata
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.