Comparison Between Auto CPAP and Fixed CPAP in Chinese Patients With OSA
NCT ID: NCT00307424
Last Updated: 2006-03-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
INTERVENTIONAL
2004-08-31
2005-06-30
Brief Summary
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Detailed Description
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Randomization:
Arm 1: auto CPAP sleep study then auto CPAP for 2 months Arm 2: fixed CPAP titration then fixed CPAP for 2 months
Then switch over to the other arm
Trial end after 4 months, compliance and other parameters would be compared between two arms as described in the endpoint session.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
NONE
Interventions
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AutoCPAP
FixCPAP
Eligibility Criteria
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Inclusion Criteria
* OSA confirmed with sleep study
* Presence of daytime symptoms with excessive daytime sleepiness
* Age between 18 to 65
* RDI greater than 30
* Agreed to participate in trial with informed consent signed
Exclusion Criteria
* Patients with known COPD with type II failure
* Patients with known heart failure.
* Patients with predominant central sleep apnea.
* Patients need bilevel positive airway pressure ventilation.
* Patients refusing to participate the trial.
* Patients have difficulty to follow up regularly.
* patients with untreated or under treatment of hypothyroidism
18 Years
65 Years
ALL
No
Sponsors
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Chinese University of Hong Kong
OTHER
Principal Investigators
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To K Wang, FHKCP
Role: PRINCIPAL_INVESTIGATOR
Prince of Wales Hosptial
Locations
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North District Hospital
Hong Kong, , China
Prince of Wales Hospital
Hong Kong, , China
Countries
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References
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To KW, Chan WC, Choo KL, Lam WK, Wong KK, Hui DS. A randomized cross-over study of auto-continuous positive airway pressure versus fixed-continuous positive airway pressure in patients with obstructive sleep apnoea. Respirology. 2008 Jan;13(1):79-86. doi: 10.1111/j.1440-1843.2007.01138.x.
Other Identifiers
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CRE-2004.258-T
Identifier Type: -
Identifier Source: org_study_id