A clinical study to evaluate the effect of oral appliance on sleep apnea syndrome
Not Applicable
Recruiting
- Conditions
- obstractive sleep apnea
- Registration Number
- JPRN-UMIN000049236
- Lead Sponsor
- Tohoku University Graduate School of Dentistry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Patients with temporomandibular disorder (2) Patients undergoing orthodontic treatment (3) Patients with severe periodontal disease (4) Patients with low compliance to OA (5) Patients with allergies to floor resin (6) Women who are pregnant, possibly pregnant, within 28 days after childbirth (7) Patients who are diagnosed to be difficult to participate in the study due to complication of psychosis or psychiatric symptoms (8) Others
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the reduction rate of the apnea hypopnea index
- Secondary Outcome Measures
Name Time Method