Evidence map›Paper›PMID 26489663›Full record

Trial reportBMC psychiatry2015

Study protocol for the randomised controlled trial: Ketamine augmentation of ECT to improve outcomes in depression (Ketamine-ECT study).

Liam Trevithick, R Hamish McAllister-Williams, Andrew Blamire, Tim Branton, Ross Clark, Darragh Downey, Graham Dunn, Andrew Easton, Rebecca Elliott, Clare Ellwell and 11 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in BMC psychiatry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
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

21 authors at 10 institutions in 2 countries.

Liam TrevithickInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK. liam.trevithick@newcastle.ac.uk.
R Hamish McAllister-WilliamsInstitute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK. hamish.mcallister-williams@newcastle.ac.uk.
Andrew BlamireInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK. andrew.blamire@newcastle.ac.uk.
Tim BrantonLeeds and York Partnership NHS Foundation Trust, Leeds, UK. t.branton@nhs.net.
Ross ClarkCentral Manchester University Hospitals NHS Foundation Trust, Manchester, UK. rossclark@doctors.org.uk.
Darragh DowneyNeuroscience and Psychiatry Unit, The University of Manchester and Manchester Academic Health Science Centre, Room G809, Stopford Building, Oxford Road, Manchester, M13 9PT, UK. darragh.downey@manchester.ac.uk.
Graham DunnBiostatistics Group, The University of Manchester, Manchester, UK. graham.dunn@manchester.ac.uk.
Andrew EastonAlpha Hospital, Sheffield, UK. amee100@doctors.org.uk.
Rebecca ElliottNeuroscience and Psychiatry Unit, The University of Manchester and Manchester Academic Health Science Centre, Room G809, Stopford Building, Oxford Road, Manchester, M13 9PT, UK. rebecca.elliot@manchester.ac.uk.
Clare EllwellBiomedical Optics Research Laboratory, University College London, London, UK. celwell@medphys.ucl.ac.uk.
Katherine HaydenPennine Care NHS Foundation Trust, Stockport, UK. Katherine.hayden@nhs.net.
Fiona HollandBiostatistics Group, The University of Manchester, Manchester, UK. fiona.holland@manchester.ac.uk.
Salman KarimLancashire Care NHS Foundation Trust/ The University of Manchester, Preston, UK. salman.karim@manchester.ac.uk.
Jo LoweNeuroscience and Psychiatry Unit, The University of Manchester and Manchester Academic Health Science Centre, Room G809, Stopford Building, Oxford Road, Manchester, M13 9PT, UK. jo.e.lowe@manchester.ac.uk.
Colleen LooSchool of Psychiatry, University of New South Wales, Sydney, Australia. colleen.loo@unsw.edu.au.
Rajesh NairTees, Esk and Wear Valley NTW NHS Foundation Trust, Darlington, UK. rajesh.nair1@nhs.net.
Timothy OakleyNorthumberland Tyne and Wear NHS Foundation Trust, Newcastle upon Tyne, UK. tim.oakley@ntw.nhs.uk.
Antony PrakashDerbyshire Healthcare NHS Foundation Trust, Derby, UK. Antony.Prakash@derbyshcft.nhs.uk.
Parveen K SharmaManchester Mental Health and Social Care Trust, Manchester, UK. parveen.sharma@mhsc.nhs.uk.
Stephen R WilliamsImaging Science and Biomedical Imaging Institute, The University of Manchester, Manchester, UK. steve.williams@manchester.ac.uk.
Ian M AndersonNeuroscience and Psychiatry Unit, The University of Manchester and Manchester Academic Health Science Centre, Room G809, Stopford Building, Oxford Road, Manchester, M13 9PT, UK. ian.anderson@manchester.ac.uk.
University of Manchester · GBNewcastle University · GBManchester Academic Health Science Centre · GBCumbria Northumberland Tyne and Wear NHS Foundation Trust · GBLancashire Care NHS Foundation Trust · GBLeeds and York Partnership NHS Foundation Trust · GBPennine Care NHS Foundation Trust · GBTees, Esk and Wear Valleys NHS Foundation Trust · GBUniversity College London · GBUNSW Sydney · AU

Funding

Medical Research Council MC_PC_12036Medical Research Council MR/K000608/1
6 · The paper itself

Abstract

backgroundThere is a robust empirical evidence base supporting the acute efficacy of electroconvulsive therapy (ECT) for severe and treatment resistant depression. However, a major limitation, probably contributing to its declining use, is that ECT is associated with impairment in cognition, notably in anterograde and retrograde memory and executive function. Preclinical and preliminary human data suggests that ketamine, used either as the sole anaesthetic agent or in addition to other anaesthetics, may reduce or prevent cognitive impairment following ECT. A putative hypothesis is that ketamine, through antagonising glutamate receptors, protects from excess excitatory neurotransmitter stimulation during ECT. The primary aim of the ketamine-ECT study is to investigate whether adjunctive ketamine can attenuate the cognitive impairment caused by ECT. Its secondary aim is to examine if ketamine increases the speed of clinical improvement with ECT. METHODS/

designThe ketamine ECT study is a multi-site randomised, placebo-controlled, double blind trial. It was originally planned to recruit 160 moderately to severely depressed patients who had been clinically prescribed ECT. This recruitment target was subsequently revised to 100 patients due to recruitment difficulties. Patients will be randomly allocated on a 1:1 basis to receive either adjunctive ketamine or saline in addition to standard anaesthesia for ECT. The primary neuropsychological outcome measure is anterograde verbal memory (Hopkins Verbal Learning Test-Revised delayed recall task) after 4 ECT treatments. Secondary cognitive outcomes include verbal fluency, autobiographical memory, visuospatial memory and digit span. Efficacy is assessed using observer and self-report efficacy measures of depressive symptomatology. The effects of ECT and ketamine on cortical activity during cognitive tasks will be studied in a sub-sample using functional near-infrared spectroscopy (fNIRS). DISCUSSION: The ketamine-ECT study aims to establish whether or not adjunctive ketamine used together with standard anaesthesia for ECT will significantly reduce the adverse cognitive effects observed after ECT. Potential efficacy benefits of increased speed of symptom improvement and a reduction in the number of ECT treatments required will also be assessed, as will safety and tolerability of adjunctive ketamine. This study will provide important evidence as to whether adjunctive ketamine is routinely indicated for ECT given for depression in routine NHS clinical practice.

trial registrationCurrent Controlled Trials: ISRCTN14689382 (assigned 30/07/2012); EudraCT Number: 2011-005476-41.

Indexed as

AdolescentAdultAgedCognitionCognition DisordersCombined Modality TherapyDepressive Disorder, Treatment-ResistantDouble-Blind MethodElectroconvulsive TherapyExcitatory Amino Acid AntagonistsExecutive FunctionHumansKetamineMajor Depressive DisorderMemory, EpisodicMental RecallExcitatory Amino Acid AntagonistsKetamine

Identifiers

PMID26489663
PMCPMC4618126
OpenAlexW2171368733

What OpenQuestion holds

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LicenceCC BY
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.