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Trial registered on ANZCTR
Registration number
ACTRN12606000262505
Ethics application status
Approved
Date submitted
26/06/2006
Date registered
28/06/2006
Date last updated
28/06/2006
Type of registration
Prospectively registered
Titles & IDs
Public title
Technical reliability and accuracy of home polysomnography to diagnose obstructive sleep apnoea
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Scientific title
Technical reliability and accuracy of home polysomnography to diagnose obstructive sleep apnoea
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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:
Obstructive Sleep Apnoea
1238
0
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Condition category
Condition code
Respiratory
1323
1323
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0
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Sleep apnoea
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Randomised study of laboratory versus home based polysomnography (PSG). Subjects receive 2 laboratory (compumedics S series sleep system) and 1 home PSG (COmpumedics Siesta sleep system) over a 2 week period. Subjects are their own controls.
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Intervention code [1]
1129
0
Treatment: Devices
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
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Apnoea Hypopnoea Index
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Assessment method [1]
1809
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Timepoint [1]
1809
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During overnight PSG
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Secondary outcome [1]
3172
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Arousal Index
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Assessment method [1]
3172
0
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Timepoint [1]
3172
0
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Secondary outcome [2]
3173
0
Desaturation index
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Assessment method [2]
3173
0
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Timepoint [2]
3173
0
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Secondary outcome [3]
3174
0
% signal loss
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Assessment method [3]
3174
0
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Timepoint [3]
3174
0
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Secondary outcome [4]
3175
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Patient preference
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Assessment method [4]
3175
0
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Timepoint [4]
3175
0
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Secondary outcome [5]
3176
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Diagnostic confidence for each of the 3 over night PSG studies.
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Assessment method [5]
3176
0
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Timepoint [5]
3176
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Eligibility
Key inclusion criteria
Adult subjects referred from Sleep Clinic for PSG to confirm / exclude diagnosis of OSA.
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Minimum age
18
Years
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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
Lives outside Home PSG zone, referral for alternate sleep disorder, Respiratory Failure, Renal Failure, Pyschiatric Disorder.
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Study design
Purpose of the study
Diagnosis
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Concealed urn randomisation
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Two options- equal number of slips in urn of option 1 and option2
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/07/2006
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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
30
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
337
0
New Zealand
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State/province [1]
337
0
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Funding & Sponsors
Funding source category [1]
1452
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University
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Name [1]
1452
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Otago University Mini Research Grant
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Address [1]
1452
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Country [1]
1452
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New Zealand
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Primary sponsor type
University
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Name
Otago University
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Address
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Country
New Zealand
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Secondary sponsor category [1]
1281
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None
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Name [1]
1281
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Nil
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Address [1]
1281
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Country [1]
1281
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
2828
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WellSleep
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Ethics committee address [1]
2828
0
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Ethics committee country [1]
2828
0
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Date submitted for ethics approval [1]
2828
0
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Approval date [1]
2828
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16/03/2006
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Ethics approval number [1]
2828
0
CEN/05/08/061
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Summary
Brief summary
The aim of the study is to look at whether diagnosing obstructive sleep apnoea overnight at home is as reliable and accurate as diagnosing it in an attended specialised sleep laboratory overnight. Patients undergo both studt types and act as their own controls. The person analysing the overnight recordings is blinded to the patient name so that study results cannot be connected.
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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
36041
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Address
36041
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Country
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Phone
36041
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Fax
36041
0
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Email
36041
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Contact person for public queries
Name
10318
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Dr Alister Neill
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Address
10318
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Dept Medicine
Wellington School of Medicine
Wellington
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Country
10318
0
New Zealand
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Phone
10318
0
64 4 3855999
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Fax
10318
0
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Email
10318
0
[email protected]
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Contact person for scientific queries
Name
1246
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Dr Alister Neill
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Address
1246
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Department of Medicine
Wellington School of Medicine
Wellington
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Country
1246
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New Zealand
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Phone
1246
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64 4 3855999
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Fax
1246
0
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Email
1246
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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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