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Treatment of severe obstructive sleep apnea syndrome: evaluation of a therapy combining continuous positive airway pressure with an oral appliance: a pilot study

Recruiting
Conditions
'obstructive sleep apnea syndrome' and 'sleep apnea'
10046304
Registration Number
NL-OMON34972
Lead Sponsor
niversitair Medisch Centrum Groningen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

severe OSAS (AHI >30)
Age > 20 years.

Exclusion Criteria

Medical and psychological exclusion:
1. Morphologic abnormalities of the upper airway
2. Endocrine dysfunction
3. Reported or documented severe cardiac- or pulmonary co-morbidity
4. Psychiatric disorders
Dental exclusion for Oral Appliance therapy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The feasibility for planning a main randomised controlled study to compare<br /><br>OA-CPAP with CPAP alone.<br /><br>Patient*s satisfaction to an OA-CPAP with a questionnaire.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>An ambulant polysomnography will be assessed for the AHI (efficacy), arousals,<br /><br>sleep stages and oxyhemoglobin saturation.<br /><br>Compliance is operationalized by assessing the number of hours per night and<br /><br>the number of nights per week that the device is used (questionnaire).<br /><br>Side-effects, EDS (excessive daytime sleepiness ) and neurobehavioral outcomes<br /><br>will also be evaluated with a questionnaire. </p><br>
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