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Trial registered on ANZCTR
Registration number
ACTRN12613000373774
Ethics application status
Approved
Date submitted
28/03/2013
Date registered
8/04/2013
Date last updated
9/04/2013
Type of registration
Retrospectively registered
Titles & IDs
Public title
The clinical efficiency of positive airway pressure (PAP) treatment in patients with moderate-severe obstructive sleep apnea syndrome (OSAS)
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Scientific title
A study evaluating the clinical efficiency and compliance of positive airway pressure (PAP) treatment on patients with moderate-severe obstructive sleep apnea syndroma (OSAS)
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Secondary ID [1]
282207
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Nil
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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
289081
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0
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Sleep apnoea
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Arm 1: device
(In moderate-severe OSAS patients main treatment is positive airway pressure (PAP) device. We have investigated the efficiancy of this device.)
In obstructive sleep apnea patients the saturation of oxygen level are under normal level. In some patients we measure that about 30-40% PAP device positive pressure. Low oxygen levels are associated with chronic disease as myocardial infarction. When apnea appears in patients and saturation of the oxygen level decreases PAP device improve saturation of oxygen by positive pressure. Patients should use the device every night. Patients who are using the device for more than 6 months (between 6-12months) will be observed.
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Intervention code [1]
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Not applicable
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Comparator / control treatment
In this study we just observed the patients using positive airway pressure device-This is an observational study.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Positive airway pressure therapy provides significant improvements in sleep and quality of life.
We use questionnaire method to maintain this knowledge.
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Assessment method [1]
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Timepoint [1]
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At 6 months after patients have begun using PAP
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Secondary outcome [1]
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When evaluating the efficiancy of positive airway pressure treatment we used Epworth Sleepines Scale (ESS) and 2 other questionnaire which we prepared for Turkish patients. This kind of questionarre could be used in these syudies.
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Assessment method [1]
302005
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Timepoint [1]
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At 6 months after patients have begun using PAP
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Eligibility
Key inclusion criteria
Obstruvtive Sleep Apnea patients with AHI>5 (apnea hypopnea index)
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Minimum age
18
Years
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Maximum age
75
Years
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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
AHI<5 (apnea hypopnea index)
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Study design
Purpose
Screening
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Duration
Longitudinal
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Selection
Defined population
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Timing
Retrospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
1/01/2008
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Actual
1/01/2008
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Date of last participant enrolment
Anticipated
1/04/2011
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Actual
1/04/2011
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
75
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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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Turkey
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State/province [1]
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ankara
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Address [1]
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Country [1]
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Turkey
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Primary sponsor type
Individual
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Name
Sabri Koseoglu
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Address
Mebusevleri Mahallesi, Iller sokak,12/05 tandogan ANKARA
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Country
Turkey
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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]
285760
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Country [1]
285760
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Ankara Numune Education and Research Hospital Ethical Committee
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Ethics committee address [1]
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Talatpasa blvd. No:5 Altindag Ankara 06100
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Ethics committee country [1]
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Turkey
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Date submitted for ethics approval [1]
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01/01/2013
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Approval date [1]
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14/01/2013
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Ethics approval number [1]
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551/2013
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Summary
Brief summary
Objectives: The aim of this study was to evaluate the clinical efficiency and compliance of positive airway pressure treatment. Materials&Methods: This study was conducted on moderate-severe obstuctive sleep apnea syndrome (OSAS) patients who admitted to Ankara Numune Hospital Sleep Center between 2008 and 2012. Seventy five patients with moderate-severe OSAS who were using PAP treatment regularly were enrolled to study. Patient’s usage data, Epworth sleepiness scale (ESS) scores and the differences in complaints of OSAS were recorded. Results: The overall complaints were improved when compared to pretreatment period. Particularly there was improvement in apnea, snoring, excessive daytime sleepiness, fatigue and sleep quality. Conclusion: PAP is effective in reducing symptoms in people with moderate and severe OSAS. To inform the patients in details and creation of strategies for close follow up are necessary for improving the compliance of the patients.
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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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Dr Sabri Koseoglu
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Address
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Mebusevleri Mahallesi , Iller Sok, 12/5, 06640, Tandogan/ANKARA
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Country
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Turkey
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Phone
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+905056459911
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Sabri Koseoglu
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Address
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Mebusevleri Mahallesi , Iller Sok, 12/5, 06640, Tandogan/ANKARA
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Country
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Turkey
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Phone
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+905056459911
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Fax
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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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sabri Koseoglu
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Address
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Mebusevleri Mahallesi , Iller Sok, 12/5, 06640, Tandogan/ANKARA
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Country
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Turkey
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Phone
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+905056459911
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Fax
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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
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Study results article
Yes
April 29 2013
Documents added automatically
Source
Title
Year of Publication
DOI
Dimensions AI
The Clinical Efficiency of Positive Airway Pressure Treatment
2013
https://doi.org/10.1155/2013/245476
N.B. These documents automatically identified may not have been verified by the study sponsor.
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