Researchers look at therapeutic benefits of ketamine
The largest trial into the use of Electroconvulsive Therapy (ECT) in the UK in more than 30 years will look into how the use of the Class C drug ketamine might reduce the side effects of ECT for those being treated for severe depression.
Both ECT and ketamine are both known to have benefits as antidepressants and as rapid and effective treatments for Treatment Resistant Depression (TRD).
However ECT can be associated with confusion and impaired thinking ability and memory. Ketamine, also known by its street name of ‘Special K’, is used as an animal and human anaesthetic and sometimes for pain relief but cannot be used on its own as a treatment for depression. Small studies have suggested that combining ketamine with ECT can protect against the detrimental effects of ECT on thought processes and hasten the speed of getting better from depression, but a proper large scale trial of the combination is needed before it is used in clinical practice.
It is particularly hoped that ketamine will reduce the longer-term loss of past memories, including autobiographical memory – which may include memories of childhood holidays, growing up and early life – that some people experience with ECT and which can be very distressing. The researchers also want to know whether ketamine will increase the rate improving depressive symptoms, which may mean that fewer ECT treatments are needed. An optional part of the study will be to include brain imaging to understand better how ketamine might be working in the brain.
Project manager Jo Lowe of The University of Manchester is coordinating the research team, which is led by Professor Ian Anderson, and the trial is sponsored by Manchester Mental Health and Social Care Trust with the study involving an additional five NHS Trusts and three universities in the UK.
Professor Anderson said: “It’s a great opportunity to really study ECT and see how we can improve it. ECT is the most effective treatment we have for severe and Treatment Resistant Depression – but it can cause cognitive and memory difficulties as a side-effect. This is one of the reasons why not everyone who could benefit from ECT receives it, or is even offered the opportunity to have it. We believe that by combining ketamine with ECT these side effects on thinking and memory will be reduced or even prevented completely. This may make ECT a more acceptable option in the future.”
Ketamine will be given alongside the anaesthetic received during ECT, and those taking part in the study will be randomised to either receive ketamine, or a placebo (dummy) injection.
Recruitment has just started for the trial, which is looking for 160 participants, all of whom will need to have been referred for ECT by their consultant. Those who do take part in the clinical research trial will help researchers find out whether ketamine should be given routinely with ECT and may help develop better treatments in the future. Participants may also experience direct benefit from less cognitive impairment after ECT and perhaps a faster improvement in their depression (if they receive ketamine),
If you would like to find out more about the study, please visit the website.
If you are referring someone for ECT, or caring for someone considering ECT, please contact the trial on 0161 275 1235 or KetECT@manchester.ac.uk
Notes for editors
Manchester Mental Health and Social Care Trust provides a wide spectrum of mental health, physical health and wellbeing services. It is one of only five combined mental health and social care Trusts in England and Wales. The Trust serves an estimated population of 503,000 people, operating with the Manchester City Council boundaries.
For more information contact Judith King on 0161 882 1382 or e mail: Judith.email@example.com
This release relates to independent research funded by the Medical Research Council (MRC) and managed by the Efficacy and Mechanism Evaluation (EME) programme of the National Institute for Health Research (NIHR) on behalf of the MRC-NIHR partnership.
The views expressed in this publication are those of the author(s) and not necessarily those of the MRC, NHS, EME, NIHR or the Department of Health.