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se of upper airway measurements for the prediction of successful mandibular advancement device therapy both in protrusion and retraction of the mandible in patients with obstructive sleep apnoea.

Completed
Conditions
Sleep Apnea
upper airway collapse
10046304
Registration Number
NL-OMON48021
Lead Sponsor
Medisch Spectrum Twente
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
25
Inclusion Criteria

Obstructive sleep apnea patients with an apnea-hypopnea index equal or bigger than 15
Written informed consent prior to participation.
Scheduled a control poly(somno)graph after titration of MAD therapy or have had a control poly(somno)graph within the last year and a half year after titration of MAD therapy.

Exclusion Criteria

Inability to read and/or understand the Dutch language
Having a control polygraph after an initial polysomnography
Having a control polysomnography after an initial polygraph

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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