Outcome assessment of Type I Tympanoplasty using varied thickness tragal cartilage as graft material
Not Applicable
- Conditions
- Health Condition 1: H653- Chronic mucoid otitis mediaHealth Condition 2: H661- Chronic tubotympanic suppurative otitis media
- Registration Number
- CTRI/2024/05/066903
- Lead Sponsor
- Datta Meghe Institute of Higher Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with COM from 12-50 years with intact ossicular chain
Exclusion Criteria
1) Children below the age group of 12 years and more than 50 years old
2) Patients with unsafe COM
3) Patients with SNHL, Mixed hearing loss
4) Patients with ossicular discontinuity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the outcomes of hearing (by pure tone audiometry) and graft uptake (by otoendoscopic picture) in study groups of patients operated with Type I Tympanoplasty using varied thickness tragal cartilage as graft materialTimepoint: These outcomes will be evaluated within the duration of 3 weeks, 6 weeks and 3 months
- Secondary Outcome Measures
Name Time Method To compare clinical outcome of Type 1 Tympanoplasty using varied thickness tragal cartilage .Timepoint: 2 years