NCT00226876

Completed

Dreaming During Anaesthesia and Anaesthetic Depth

Melbourne Health Source

Other study identifiers

Sponsor study identifier

2005/016

Study Type

observational

Actual enrollment (reported)

300

Locations

1 country

Sites

3

Timeline

Study Start

February 2005

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

March 2006

Actual (reported)

Study Completion

March 2006

Actual (reported)

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).

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 300 participants
Study completion date: March 2006
Actual (reported)
Listed locations: 1 countries · 3 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
February 2005
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
September 26, 2005
Actual (reported)
First Posted
September 27, 2005
Actual (reported)
Primary Completion
March 2006
Actual (reported)
Study Completion
March 2006
Actual (reported)

Last Updated: May 30, 2013
Status Verified: September 2005
Last Update Submitted: May 28, 2013

Conditions

Anaesthesia

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:

Sponsors & Collaborators

Melbourne Health
Otherlead
Australian and New Zealand College of Anaesthetists
Othercollaborator

Study Sites (3)

Royal Melbourne Hospital

Melbourne, Victoria, 3050, Australia

King Edward Memorial Hospital for Women

Perth, Western Australia, 6000, Australia

Royal Perth Hospital

Perth, Western Australia, 6000, Australia

Study Officials

Kate Leslie, MD
Melbourne Health
PRINCIPAL INVESTIGATOR

Enrollment

300 participants (actual enrollment reported by the registry).

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 2005

Date type not reported

This date has not been verified as actual or estimated.

NCT00521612

Sevoflurane vs. Isoflurane for Low-Flow General Anaesthesia for Abdominal Surgery

Not ApplicableCompleted

NCT01142635

Electromyographic (EMG) on the Anaesthesia Monitor

Phase 4Completed

NCT00919126

General Anesthesia With Xenon in Inspiratory Concentrations of 50% and 70% and Total I.V. Anaesthesia.

Phase 3Terminated

NCT02248623

Intraoperative Anaesthesia Awareness Following Induction of Anaesthesia

Completed

NCT01076790

Dexmedetomidine-propofol-remifentanil Anaesthesia and Reactivity to Noxious Stimuli

Phase 4Completed

NCT02920749

Study of Anaesthesia Costs and Recovery Profiles

Not ApplicableCompleted

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.

Primary Completion

March 2006

Actual (reported)

Study Completion

March 2006

Actual (reported)

Last Updated

May 30, 2013

Record last verified: 2005-09

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00226876
Data provider: ClinicalTrials.gov
Source updated: 2013-05-30
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:40:24 UTC

Locations

AU(3)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (3)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations