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Ketamine as an Anaesthetic Agent in Electroconvulsive Therapy (ECT)

A Double-blind Randomised, Placebo-controlled Study of Adjunctive Ketamine Anaesthesia in ECT (Electroconvulsive Therapy)

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00680433
Enrollment
83
Registered
2008-05-20
Start date
2008-04-30
Completion date
2012-10-31
Last updated
2013-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Episode

Brief summary

Research into the mechanisms underlying memory impairment in ECT suggests that its development may be prevented by the administration of certain medications at the time of ECT treatment. For example there are reasons to believe that ketamine, also used as an anaesthetic agent, may have such protective properties. In this clinical study patients undergoing a course of ECT will be offered the opportunity to receive a small dose of ketamine (or a placebo) as part of their anaesthetic at the time of ECT treatment. Mood changes and any memory changes will be evaluated to see if the subjects who received ketamine had less memory side effects than those who did not, while still improving their depression.

Detailed description

This study will report on two related trials. In the outpatient trial, patients will be administered adjunctive ketamine at two different doses (0.25mg/kg; 0.5mg/kg), and a placebo (saline), across 3 consecutive sessions within their regular maintenance ECT course. The order of conditions will be randomised across participants. Patients will be required to learn some words and faces 20 minutes prior to ECT, and complete a detailed cognitive battery 4 hours after ECT on each of the 3 occasions. The purpose of this trial is to determine whether ketamine is superior to placebo in reducing cognitive impairment following ECT and what the optimal dose of ketamine is for minimising cognitive and other side effects. Projected sample for this trial is N = 17. In the inpatient trial, patients will be randomly assigned to receive ketamine or placebo for the duration of the acute ECT course. Patients will be administered a detailed cognitive battery the day before commencing ECT treatment, the day after the 6th treatment, and 1-3 days and 1 month following the end of the acute ECT course. The purpose of this trial is to examine whether patients in the ketamine condition had superior cognitive outcomes to those in the placebo condition during and following a course of ECT. In addition, depressive symptomatology will be examined throughout the ECT course to determine whether ketamine anaesthesia during ECT has antidepressant, as well as, cognitive benefits. Projected sample for this trial is N = 34. This entry gives details of the main clinical trial: The effects of ketamine across a course of ECT.

Interventions

DRUGKetamine

Ketamine IV will be administered after the administration of the normal anaesthetic agents for ECT.

DRUGSaline

Saline (placebo) will be administered after the normal anaesthetic agents in ECT.

Sponsors

Wesley Mission
CollaboratorOTHER
Northside Clinic, Australia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Satisfy DSM-IV-TR criteria for Major Depressive Episode * 18 years or over * Does not have a diagnosis of schizophrenia, schizoaffective disorder, rapid cycling bipolar disorder, or current psychotic symptoms * No known sensitivity to ketamine * No ECT in the last 3 months * No drug or alcohol abuse in the last 12 months * Able to give informed consent * Score at least 24 on Mini Mental State Examination

Design outcomes

Primary

MeasureTime frame
Memory testsBefore ECT, after 6 ECT treatments, at the end of the ECT course

Secondary

MeasureTime frame
Depression rating scaleBefore ECT, after each week of treatment, at the end of the ECT course

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026