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Evaluation of mandibular advancement device with high compliance rate for obstructive sleep apnea patient

Not Applicable
Conditions
obstructive sleep apnea syndrome
Registration Number
JPRN-UMIN000018643
Lead Sponsor
Kyushu Dental University
Brief Summary

Discomfort caused by the oral appliance was greater for the soft type appliance than for the hard type appliance in the following patient assessed variables: Dry mouth; Ill fitting appliance and Difficulty sleeping. Only two patient exhibited a complete match between results of sleep data and the type of oral appliance that the patient wanted to continue using.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
7
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients who has underwent other treatment for OSAS 2. Patients with central sleep apnea dominance (CAI >5/hr) 3. Patients with other sleep disorders 4. Patients with mental disorders 5. Patients with craniofacial disorders 6. Patients with multiple teeth loss

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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