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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ANZCTR
Last refreshed on: 13 January 2020
Main ID:  ACTRN12605000307606
Date of registration: 06/09/2005
Prospective Registration: Yes
Primary sponsor: Melbourne Health
Public title: Dreaming during anaesthesia and anaesthetic depth
Scientific title: Dreaming during anaesthesia and anaesthetic depth
Date of first enrolment: 16/08/2006
Target sample size: 300
Recruitment status: Completed
URL:  https://anzctr.org.au/ACTRN12605000307606.aspx
Study type:  Observational
Study design:  Purpose: Screening;Duration: Longitudinal;Selection: Defined population;Timing: Prospective;  
Phase:  Not Applicable
Countries of recruitment
Australia
Contacts
Name: Mrs Associate Professor Kate Leslie   
Address:  Department of Anaesthesia and Pain Management Royal Melbourne Hospital Parkville VIC 3050 Australia
Telephone: +61 3 93427000
Email: kate.leslie@mh.org.au
Affiliation: 
Name: Prof Associate Professor Kate Leslie   
Address:  Department of Anaesthesia and Pain Management Royal Melbourne Hospital Parkville VIC 3050 Australia
Telephone: +61 3 93427000
Email: kate.leslie@mh.org.au
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: ASA 1-2, presenting for surgery under relaxant GA.
Exclusion criteria: Patients without adequate English language comprehension, or who have major psychiatric or drug abuse problems excluded.

Age minimum: Not stated
Age maximum: Not stated
Gender: Both males and females
Health Condition(s) or Problem(s) studied
Dreaming during anaesthesia;
Dreaming during anaesthesia
Anaesthesiology - Other anaesthesiology
Intervention(s)
Observational study of anaesthetic depth in patients who do and do not report dreaming.
Primary Outcome(s)
Anaesthetic depth[Measured from anaesthetic induction until the first postoperative interview when patient responds to command]
Secondary Outcome(s)
Quality of recovery[ Measured at 2 hours and 24 hours postoperatively.]
Secondary ID(s)
Nil known
Source(s) of Monetary Support
ANZCA
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Royal Melbourne Hospital
Status: Not approved
Approval date:
Contact:
King Edward Memorial Hospital for Women
Status: Not approved
Approval date:
Contact:
Royal Perth Hospital
Results
Results available:
Date Posted:
Date Completed:
URL:
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