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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02541214
Registration number
NCT02541214
Ethics application status
Date submitted
1/09/2015
Date registered
4/09/2015
Date last updated
2/08/2019
Titles & IDs
Public title
Evaluation of a Nasal Mask for the Treatment of Obstructive Sleep Apnea in New Zealand
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Scientific title
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Secondary ID [1]
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CIA-171
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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 Apnea
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Condition category
Condition code
Respiratory
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Sleep apnoea
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Experimental: Trial Nasal Mask - The participant will use the Saturn nasal mask for 2 weeks in home
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Subjective measurements of comfort on the trial Nasal Mask gathered through a custom questionnaire
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Assessment method [1]
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Timepoint [1]
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2 weeks in home
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Secondary outcome [1]
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Seal performance of the trial Nasal mask as measured by the subjective perception of leak through a custom questionnaire, in addition to objective leak data and treatment efficacy through the Positive Airway Pressure therapy device.
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Assessment method [1]
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the participant would choose from a 5 point likert scale on a questionnaire. The scale range from "very good" to "very poor"
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Timepoint [1]
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2 weeks in home
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Secondary outcome [2]
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Objective leak data through the Positive Airway Pressure therapy device
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Assessment method [2]
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Evaluating the leak of the trial Nasal mask
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Timepoint [2]
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2 weeks in home
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Secondary outcome [3]
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Treatment efficacy through the Positive Airway Pressure therapy device
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Assessment method [3]
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Evaluating the number of apnea/hypopnea per hour
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Timepoint [3]
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2 weeks in home
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Secondary outcome [4]
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Preference of the Trial Nasal mask compared to the participant's usual mask through a custom questionnaire.
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Assessment method [4]
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the participant would either choose the trial Nasal mask or their usual mask as their primary mask
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Timepoint [4]
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2 weeks in home
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Eligibility
Key inclusion criteria
* Aged 18+
* Diagnosed with Ostructive Sleep Apnea by a practicing physician or clinicans
* Existing nasal or nasal pillows user
* Prescribed Positive Airway Pressure therapy (Bi-Level or Continuous Positive Airway Pressure (CPAP) or Automatic Positive Airway Pressure (APAP))
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Minimum age
18
Years
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Maximum age
No limit
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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
* Inability to give informed consent
* Pregnant or think they may be pregnant
* Anatomical or physiological conditions making Positive Airway Pressure therapy inappropriate (e.g unconsolidated facial fracture)
* Patients who are in a coma or decreased level of consciousness
* Current diagnosis of CO2 retention
* Commercial Drivers who are investigated by New Zealand Transport Agency (NZTA)
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Study design
Purpose of the study
Treatment
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Allocation to intervention
NA
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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
NA
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/09/2015
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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
1/11/2015
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Sample size
Target
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Accrual to date
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Final
39
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Recruitment in Australia
Recruitment state(s)
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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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Hamilton
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Country [2]
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New Zealand
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State/province [2]
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Hastings
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Fisher and Paykel Healthcare
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Currently, Fisher and Paykel Healthcare (FPH) is developing a new nasal mask. This investigation is designed to evaluate the performance of the trial nasal mask, focused specifically on how the different seal sizes will perform on Obstructive Sleep Apnea participants who are currently on Positive Airway Pressure therapy. Participant's prescribed treatment pressure with their usual mask will be collected for 7 days ± 3 days prior to mask fitting with the trial nasal mask. They will then be issued with the trial nasal mask to use in-home for 14 days ± 4 days.
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Trial website
https://clinicaltrials.gov/study/NCT02541214
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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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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 scientific queries
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
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT02541214
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