Evaluation of the usefulness and safety of the combined use of an ear prosthesis and a cartilage conduction hearing aid
Not Applicable
Recruiting
- Conditions
- Patients with unilateral or bilateral auricular defects, including microtia who use the cartilage conduction hearing aid
- Registration Number
- JPRN-UMIN000044711
- Lead Sponsor
- Keio University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Patients who have allergic reactions to cartilage conduction hearing aids, ear prostheses, adhesive agents, skin protectants, or removers; (2) Patients who have difficulty in performing pure tone audiometry and speech intelligibility tests; (3) When the principal investigator or sub-investigator judges that participation in this study is not appropriate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method