Cognitive Recovery After Electroconvulsive Therapy and General Anesthesia
Single-blinded, randomised, crossover trial (n=17) in treatment-resistant depression comparing etomidate- vs ketamine-general anaesthesia with ECT and ketamine alone; ketamine ~2 mg/kg IV across six treatment sessions per participant.
Detailed Description
This study characterises recovery of brain activity and cognitive function following electroconvulsive therapy (ECT) and general anaesthesia using ketamine or etomidate in patients with treatment-resistant depression.
Design: single-blinded, randomised crossover. After a titration ECT session with etomidate, participants undergo six treatment sessions (three per week for two weeks) comprising etomidate+ECT, ketamine+ECT, and ketamine alone in randomized order; ketamine dosing is ~2 mg/kg.
Outcomes include cognitive assessments and EEG measures of recovery after seizure and anaesthesia to compare cognitive reconstitution and electrophysiological patterns across anaesthetic strategies.
Study Protocol
Preparation
Dosing
Integration
Study Arms & Interventions
Etomidate + ECT
active comparatorGeneral anaesthesia induced with etomidate (~0.2 mg/kg) followed by ECT at therapeutic charge.
Interventions
- Compoundvia Other• per session
Etomidate general anaesthesia ~0.2 mg/kg; ECT charge determined at titration (procedure: ECT).
- Compoundvia Other• per session
Procedure: Electroconvulsive Therapy; charge determined during titration.
Ketamine + ECT
experimentalGeneral anaesthesia induced with ketamine (~2 mg/kg) followed by ECT at therapeutic charge.
Interventions
- Ketamine2 mg/kgvia IV• per session
Ketamine general anaesthesia ~2 mg/kg (1–2.5 mg/kg range described).
- Compoundvia Other• per session
Procedure: Electroconvulsive Therapy; charge determined during titration.
Ketamine alone
active comparatorKetamine general anaesthesia without subsequent ECT charge (sham comparator).
Interventions
- Ketamine2 mg/kgvia IV• per session
Ketamine general anaesthesia ~2 mg/kg; no ECT charge administered.
Participants
Inclusion Criteria
- Inclusion Criteria:
- Treatment resistant depression requiring outpatient ECT
- Planned right unilateral ECT stimulation
- English speaking
- Able to provide written informed consent
Exclusion Criteria
- Exclusion Criteria:
- Known brain lesion or neurological illness that causes cognitive impairment
- Schizophrenia
- Schizoaffective disorder
- Blindness or deafness or motor impediments that may impair performance for cognitive testing battery
- Inadequate ECT seizure duration with etomidate
Study Details
- StatusCompleted
- PhasePhase NA
- Typeinterventional
- DesignRandomizedsingle Blind
- Target Enrollment17 participants
- TimelineStart: 2016-04-01End: 2019-09-11
- Compounds
- Topic