Development of treatment effect prediction method of oral appliance therapy for obstructive sleep apnea syndrome
Not Applicable
- Conditions
- Obstructive sleep apnea syndrome
- Registration Number
- JPRN-UMIN000014984
- Lead Sponsor
- Tokyo Medical and Dental University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 27
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients who have chronic nasal congestion, a high degree of tonsillar hypertrophy 2.Patients who will be received combined OA and nCPAP therapy 3.Patients who have received drug therapy related sleep (hypnotic, anxiolytic) 4.Diagonsed as mental disorders or temporomandibular disorders. 5.Patients who have a complication or history of respiratory disease. 6.Patients who have an allergy against steroids or vasoconstrictor. 7.Patients who need dental treatment for caries and periodontal disease in oral cavity
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method