A Clinical trial to study the efficacy of blood derived material in treating patients with ear drum perforation.
Not Applicable
- Conditions
- Health Condition 1: null- Chronic Suppurative Otitis Media - Tubo Tympanic Disease(Inactive)
- Registration Number
- CTRI/2017/04/008315
- Lead Sponsor
- Dr Nikhil Vallathukaran Mathew
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Chronic Suppurative Otiti Media- Tubotympanic Disease(Inactive)
Exclusion Criteria
Comorbities like Diabetes Mellitus, Hypertension, Bronchial Asthma, Tuberculosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess to graft uptake following application of platelet rich fibrin.Timepoint: At end of 1 week, 1 month and 3rd month
- Secondary Outcome Measures
Name Time Method To assess the hearing improvement post tympanoplastyTimepoint: At end of 3 months;To assess the rate of healing.Timepoint: At end of 1 week,1 month and 3 month