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Trial registered on ANZCTR
Registration number
ACTRN12608000005358
Ethics application status
Approved
Date submitted
27/12/2007
Date registered
7/01/2008
Date last updated
29/06/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
Angina and High Flow Oxygen
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Scientific title
A single group interventional trial of the effect of high flow oxygen on angina in patients with coronary disease
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Coronary disease
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Condition category
Condition code
Cardiovascular
2538
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0
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Coronary heart disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
High flow oxygen (administered as 15L/min via a non-rebreather mask for 30 minutes)
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Intervention code [1]
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Treatment: Other
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Comparator / control treatment
No comparator.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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First onset of definite angina replicating the subject's normal symptoms.
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Assessment method [1]
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Timepoint [1]
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Assessed during the 30 minutes the subject is receiving high flow oxygen.
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Secondary outcome [1]
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New ST segment changes greater than or equal to 1mm or T wave inversion as demonstrated by an electrocardiogram (ECG).
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Assessment method [1]
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Timepoint [1]
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Assessed during the 30 minutes the subject is receiving high flow oxygen.
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Secondary outcome [2]
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Need to stop the intervention because of any reason deemed to be of clinical concern by the attending doctor.
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Assessment method [2]
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Timepoint [2]
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Assessed during the 30 minutes the subject is receiving high flow oxygen.
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Eligibility
Key inclusion criteria
Current inpatients on the cardiac care unit (CCU) Wellington Hospital; confirmed diagnosis of coronary disease on angiography; experiencing chest pain (at rest or with minimal exertion) considered by CCU staff to be consistent with angina.
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Minimum age
Not stated
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Maximum age
Not stated
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Patients with chest pain at the time of enrolment; diagnosis of severe Chronic Obstructive Pulmonary Disease (COPD) or emphysema; room air oxygen saturations less than 92%; presence of bundle branch block pattern on resting ECG; patients requiring intravenous nitrates; glyceryl trinitrate use in the previous 2 hours.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
7/02/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
50
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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New Zealand
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State/province [1]
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Wellington
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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Medical Research Institute of New Zealand
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Address [1]
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PO Box 10055
The Terrace
Wellington
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Country [1]
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New Zealand
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Primary sponsor type
Charities/Societies/Foundations
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Name
Medical Research Institute of New Zealand
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Address
PO Box 10055
The Terrace
Wellington
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Central Regional Ethics Committee
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Ethics committee address [1]
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PO Box 5013 Wellington
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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18/06/2007
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Approval date [1]
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17/10/2007
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Ethics approval number [1]
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CEN/07/07/044
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Summary
Brief summary
It is routine clinical practice to administer high flow oxygen to patients with a heart attack or angina; however, there is some evidence to suggest that this approach may be harmful, especially in patients who are not hypoxic. This single group interventional trial aims to test this by recruiting 50 inpatients from the coronary care unit at Wellington Hospital who have confirmed coronary disease and a history of angina at rest or with minimal exertion. Subjects will receive high flow oxygen for 30 minutes. Subjects will be monitored to establish if angina occurs during the oxygen administration and if so how soon after it starts. ECGs will be taken throughout the study to monitor for any significant changes.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Kyle Perrin
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Address
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Medical Research Institute of NZ
PO Box 10055
The Terrace
Wellington
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Country
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New Zealand
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Phone
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0064 4 472 9120
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Fax
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0064 4 472 9224
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Kyle Perrin
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Address
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Medical Research Institute of NZ
PO Box 10055
The Terrace
Wellington
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Country
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New Zealand
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Phone
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0064 4 472 9120
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Fax
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0064 4 472 9224
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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