the effectiveness of the nasal airway stent (nastentTM) in sleep apnea syndrome
Not Applicable
- Conditions
- sleep apnea syndrome
- Registration Number
- JPRN-UMIN000019423
- Lead Sponsor
- Keio University school of medicine pulmonary division
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
the patients who cannot continue the use of the nasal airway stent(nastentTM) or attend a hospital
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method change of AHI after the indication of nasal airway stent(nastentTM) treatment in one month and three months
- Secondary Outcome Measures
Name Time Method frequency of adverse effect after the indication of nasal airway stent(nastentTM)in one month and three months