Comparison between two grafts in treatment of ear perforatio
Phase 4
- Conditions
- Health Condition 1: H661- Chronic tubotympanic suppurative otitis media
- Registration Number
- CTRI/2021/03/032179
- Lead Sponsor
- Department of ENT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient who gives informed and written consent.
-Patient having dry ear for atleast 6 weeks
-Patient having normal cochlear reserve
Exclusion Criteria
-Patient with active suppurative otitis media
- Patient with sensoryneural hearing loss element
- Patient with any CSOM complication, external ear pathology, sinonasal pathology.
- Patient with obvious ossicular dysfunction
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method - Graft success and failure with respect to graft material <br/ ><br>-Total hearing gain in successful graft taken up <br/ ><br>-Graft success with respect to <br/ ><br>a. size of perforation <br/ ><br>b. age and sex distribution <br/ ><br>c. duration of the diseaseTimepoint: 2 year
- Secondary Outcome Measures
Name Time Method - Graft success and failure with respect to graft material <br/ ><br>-Total hearing gain in successful graft taken up <br/ ><br>-Graft success with respect to <br/ ><br>a. size of perforation <br/ ><br>b. age and sex distribution <br/ ><br>c. duration of the diseaseTimepoint: 2 year