Effect of Subanesthetic Dose of Ketamine Combined With Propofol on Cognitive Function in Depressive Patients Undergoing Electroconvulsive Therapy
Depressive Symptoms, Impaired Cognition, Electroconvulsive Therapy
About this trial
This is an interventional treatment trial for Depressive Symptoms focused on measuring ketamine, Electroconvulsive Therapy, Cognitive Function
Eligibility Criteria
Inclusion Criteria:
- diagnosed with moderate or severe depression according to Diagnostic and Statistical Manual of Mental Disorders
- aged from 18 to 65 years old
Exclusion Criteria:
- cerebrovascular malformation, arterial aneurysm, hypertension, or glaucoma;
- classification of American Society of Anesthesiologists physical status score IV or V;
- complications such as respiratory disease, cardiovascular disease, intracranial hypertension, cerebral vascular disorder;
- presence of a foreign body such as pacemaker, intracranial electrode, and clips;
- history of seizures;
- history of drug abuse;
- concomitant presence of a mental disorder;
- pregnancy;
- history of serious adverse effects related to anesthetics;
- refusal to consent for the study, or refusal to undergo one single ECT during the first week of therapy.
- hyperthyreosis
Sites / Locations
- China,Chongqing The First Affiliated Hospital of Chongqing Medical University
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
PK group (ketamine and propofol)
P group (propofol group)
propofol 1.5 mg/kg and ketamine 0.3 mg/kg will be administered to participants separately by intravenous infusion.When patients become unconscious, succinylcholine 1 mg/kg (a muscle relaxant) will be administered intravenously. After 1 minute of succinylcholine infused, ECT will be performed with bitemporal electrode placement using a stimulus dose of 1.0-millisecond pulse width, 60-Hz frequency, 6.0-second stimulus duration, and 0.8-A maximal stimulus intensity.
propofol 1.5 mg/kg and normal saline [weight(kg)×0.3÷10]ml will be administered to participants separately by intravenous infusion.When patients become unconscious, succinylcholine 1 mg/kg (a muscle relaxant) will be administered intravenously. After 1 minute of succinylcholine infused, ECT will be performed with bitemporal electrode placement using a stimulus dose of 1.0-millisecond pulse width, 60-Hz frequency, 6.0-second stimulus duration, and 0.8-A maximal stimulus intensity.