Effect on snoring and feasibility of Nasal Airway Stent
Not Applicable
- Conditions
- Snoring
- Registration Number
- JPRN-UMIN000020662
- 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
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Patient with sleep apnea syndrome undergoing medical treatment (2) Patient with severe respiratory diseases (3) Patient with severe liver, renal, heart, etc. diseases. (4) Subject who cannot insert Nasal Airway Stent into the nasal cavity (5) Subject who cannot perform examinations (6) Subject judged as inadequate by researcher
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method (1) feasibility of using Nasal Airway Stent Before and After 4 days using Nasal Airway Stent, assessed for 3 days about (2) snoring by digital voice recorder (3) apnea and hypopnea (AHI) by Apnea hypopnea testing apparatus
- Secondary Outcome Measures
Name Time Method