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Main
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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. |
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Register:
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ANZCTR |
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Last refreshed on:
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13 January 2020 |
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Main ID: |
ACTRN12606000106538 |
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Date of registration:
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23/03/2006 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Prediction of obstructed breathing after elective surgery.
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Scientific title:
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A case control study using 12 hour continuous respiratory monitoring to assess the prediction of frequent upper airway obstructions after elective surgery by preoperative airway evaluation and risk score for obstruvtive sleep apnoea. |
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Date of first enrolment:
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01/05/2006 |
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Target sample size:
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70 |
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Recruitment status: |
Not yet recruiting |
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URL:
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https://anzctr.org.au/ACTRN12606000106538.aspx |
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Study type:
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Observational |
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Study design:
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Purpose: Screening;Duration: Longitudinal;Selection: Case control;Timing: Prospective;
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Phase:
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Not Applicable
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Countries of recruitment
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Australia
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Contacts
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Name:
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Dr Duncan W Blake
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Address:
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Department of Anaesthesia
Royal Melbourne Hospital
Grattan St
Parkville VIC 3050
Australia |
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Telephone:
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+61 3 93427925 |
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Email:
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duncan.blake@mh.org.au |
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Affiliation:
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Name:
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Dr Duncan W Blake
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Address:
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Department of Anaesthesia
Royal Melbourne Hospital
Grattan St
Parkville VIC 3050
Australia |
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Telephone:
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+61 3 93427925 |
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Email:
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duncan.blake@mh.org.au |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: Assessed prior to elective surgery, able to provide informed consent.
Exclusion criteria: Cardiac or thoracic surgery, elective postoperative ventilation, previous diagnosis of obstructive sleep apnoea and use of CPAP, day or short-stay surgery.
Age minimum:
18 Years
Age maximum:
Not stated
Gender:
Both males and females
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Health Condition(s) or Problem(s) studied
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Respiratory - Sleep apnoea
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Obstructive sleep apnoea;Postoperative respiratory obstruction;
Obstructive sleep apnoea
Postoperative respiratory obstruction
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Intervention(s)
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Continuous respiratory monitoring 8 hours with Somte portable monitor. Identification of risk factors at pre-operative assessment.
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Primary Outcome(s)
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Frequency of respiratory events per hour.[Per hour.]
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Secondary Outcome(s)
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Continuous respiratory monitoring.[Applied for 12 hours, commencing in the postoperative recovery area.]
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Association with OSA risk factors and airway examination.[Risk factors will be evaluated at the preoperative clinic, 1-2 weeks prior to surgery.]
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Source(s) of Monetary Support
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Royal Melbourne Hospital, Hospital auxilliary
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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