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Effect of Subanesthetic Dose of Ketamine Combined With Propofol on Cognitive Function in Depressive Patients Undergoing Electroconvulsive Therapy

Primary Purpose

Depressive Symptoms, Impaired Cognition, Electroconvulsive Therapy

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
ketamine and propofol
propofol and normal saline
Sponsored by
First Affiliated Hospital of Chongqing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Symptoms focused on measuring ketamine, Electroconvulsive Therapy, Cognitive Function

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. diagnosed with moderate or severe depression according to Diagnostic and Statistical Manual of Mental Disorders
  2. aged from 18 to 65 years old

Exclusion Criteria:

  1. cerebrovascular malformation, arterial aneurysm, hypertension, or glaucoma;
  2. classification of American Society of Anesthesiologists physical status score IV or V;
  3. complications such as respiratory disease, cardiovascular disease, intracranial hypertension, cerebral vascular disorder;
  4. presence of a foreign body such as pacemaker, intracranial electrode, and clips;
  5. history of seizures;
  6. history of drug abuse;
  7. concomitant presence of a mental disorder;
  8. pregnancy;
  9. history of serious adverse effects related to anesthetics;
  10. refusal to consent for the study, or refusal to undergo one single ECT during the first week of therapy.
  11. hyperthyreosis

Sites / Locations

  • China,Chongqing The First Affiliated Hospital of Chongqing Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PK group (ketamine and propofol)

P group (propofol group)

Arm Description

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.

Outcomes

Primary Outcome Measures

Mini-Mental State examination score
Mini-Mental State examination score will be measured at 24 hours after the sixth ECT.

Secondary Outcome Measures

Mini-Mental State examination score
Mini-Mental State examination score will be measured at 24 hours before the first ECT and 24 hours after each ECT, except the sixth ECT.
Effects on Antidepression (Hamilton Depression Rating Scale(HDRS)
Effect on antidepression will be measured by 24-item Hamilton Depression Rating Scale(HDRS)
Seizure Duration and Seizure Energy Index
Seizure duration and Seizure energy index will be recorded by the ECT apparatus.
Brief Psychiatric Rating Scale(BPRS)
Brief Psychiatric Rating Scale is related to psychotomimetic side-effect.
Adverse Effects include nausea, vomit, headache, tachycardia and increased blood pressure.
Adverse effects include nausea, vomit, headache, tachycardia and increased blood pressure.

Full Information

First Posted
November 19, 2014
Last Updated
December 1, 2014
Sponsor
First Affiliated Hospital of Chongqing Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT02305394
Brief Title
Effect of Subanesthetic Dose of Ketamine Combined With Propofol on Cognitive Function in Depressive Patients Undergoing Electroconvulsive Therapy
Official Title
Effect of Subanesthetic Dose of Ketamine Combined With Propofol on Cognitive Function in Depressive Patients Undergoing Electroconvulsive Therapy ---a Randomized Control Double-Blind Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Unknown status
Study Start Date
January 2015 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
February 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
First Affiliated Hospital of Chongqing Medical University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Electroconvulsive therapy (ECT) is an effective treatment for depression compared with the current antidepressant agents,but the most important side effect is cognitive dysfunction. The purpose of this study is to determine whether subanesthetic dose of ketamine combined with propofol is superior to propofol anesthesia alone in improving cognitive function in depressive patients undergoing ECT.
Detailed Description
Depression is one of the most debilitating and widespread illnesses affecting up to 20% of individuals in their lifetime. However, the current antidepressant agents take weeks to work, and fail to help at least 40% of depressed patients. Electroconvulsive therapy (ECT) is a remarkably effective treatment for depression, but its use is limited by cognitive dysfunction. As a result, it is becoming a clinical problem which need to be settled urgently. Previous clinical study showed that subanesthetic dose of ketamine could play a role in antidepressant effects with safety and minimal positive psychotic symptoms.The investigators also found that subanesthetic dose of ketamine combined with other anesthetics could improve cognitive function in depressive rats receiving electroconvulsive shock (a model for analogy with ECT). Few clinical researches concerned the effects of subanesthetic dose of ketamine combined with propofol anesthesia on cognitive function in patients after ECT, therefore the investigators conduct this randomized controlled double-blind trial. In this study, cognitive function will be rated by Mini-Mental State examination score.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Symptoms, Impaired Cognition, Electroconvulsive Therapy
Keywords
ketamine, Electroconvulsive Therapy, Cognitive Function

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
132 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PK group (ketamine and propofol)
Arm Type
Experimental
Arm Description
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.
Arm Title
P group (propofol group)
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
ketamine and propofol
Intervention Description
propofol 1.5 mg/kg and ketamine 0.3 mg/kg will be administered to participants separately by intravenous infusion.
Intervention Type
Drug
Intervention Name(s)
propofol and normal saline
Intervention Description
propofol 1.5 mg/kg and normal saline [weight(kg)×0.3÷10]ml will be administered to participants separately by intravenous infusion.
Primary Outcome Measure Information:
Title
Mini-Mental State examination score
Description
Mini-Mental State examination score will be measured at 24 hours after the sixth ECT.
Time Frame
at 24 hours after the sixth ECT
Secondary Outcome Measure Information:
Title
Mini-Mental State examination score
Description
Mini-Mental State examination score will be measured at 24 hours before the first ECT and 24 hours after each ECT, except the sixth ECT.
Time Frame
at 24 hours before the first ECT and 24 hours after each ECT, except the sixth ECT.
Title
Effects on Antidepression (Hamilton Depression Rating Scale(HDRS)
Description
Effect on antidepression will be measured by 24-item Hamilton Depression Rating Scale(HDRS)
Time Frame
at 24 hours before the first ECT and 24 hours after each ECT
Title
Seizure Duration and Seizure Energy Index
Description
Seizure duration and Seizure energy index will be recorded by the ECT apparatus.
Time Frame
at 30 seconds after each ECT
Title
Brief Psychiatric Rating Scale(BPRS)
Description
Brief Psychiatric Rating Scale is related to psychotomimetic side-effect.
Time Frame
60 minutes prior to the first ECT and at 40, 80, 110, and 230 minutes after each ECT
Title
Adverse Effects include nausea, vomit, headache, tachycardia and increased blood pressure.
Description
Adverse effects include nausea, vomit, headache, tachycardia and increased blood pressure.
Time Frame
at 40 minutes after each ECT

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Qibin Chen, Master
Phone
023-89011061
Email
403497559@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Su Min
Organizational Affiliation
First Affiliated Hospital of Chongqing Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
China,Chongqing The First Affiliated Hospital of Chongqing Medical University
City
Chongqing
State/Province
Chongqing
ZIP/Postal Code
400016
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Su Min, MD
Phone
+86-23-89011068
Email
ms89011068@163.com

12. IPD Sharing Statement

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Effect of Subanesthetic Dose of Ketamine Combined With Propofol on Cognitive Function in Depressive Patients Undergoing Electroconvulsive Therapy

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