NCT00226876

Brief Summary

Patients commonly report that they have been dreaming when they awaken from general anaesthesia. Our hypothesis is that patients who report dreaming are less deeply anaesthetised during anaesthesia than patients who do not report dreaming. Depth of anaesthesia will be determined using a processed electroencephalographic monitor (called the BIS monitor).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2005

Geographic Reach
1 country

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2005

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

September 26, 2005

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 27, 2005

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2006

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2006

Completed
Last Updated

May 30, 2013

Status Verified

September 1, 2005

Enrollment Period

1.1 years

First QC Date

September 26, 2005

Last Update Submit

May 28, 2013

Conditions

Keywords

dreaminganaesthesiaelectroencephalographybispectral indexawareness

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Patients presenting for elective non-cardiac surgery

You may qualify if:

  • Age 18-50 years
  • American Society of Anesthesiologists physical status 1-3
  • Non-cardiac surgery under relaxant general anaesthesia
  • Tracheal extubation planned at end of surgery

You may not qualify if:

  • Inadequate English language skills (due to language barrier, cognitive deficit or intellectual disability)
  • Major drug abuse or psychiatric condition
  • Expected to be unable to co-operate or be available for followup

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Royal Melbourne Hospital

Melbourne, Victoria, 3050, Australia

Location

King Edward Memorial Hospital for Women

Perth, Western Australia, 6000, Australia

Location

Royal Perth Hospital

Perth, Western Australia, 6000, Australia

Location

Study Officials

  • Kate Leslie, MD

    Melbourne Health

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 26, 2005

First Posted

September 27, 2005

Study Start

February 1, 2005

Primary Completion

March 1, 2006

Study Completion

March 1, 2006

Last Updated

May 30, 2013

Record last verified: 2005-09

Locations