A Study to Compare the usefulness of two Blood Products in the Surgery of Ear Drum Perforatio
Not Applicable
- Conditions
- Health Condition 1: H729- Unspecified perforation of tympanic membraneHealth Condition 2: H729- Unspecified perforation of tympanic membrane
- Registration Number
- CTRI/2024/07/070204
- Lead Sponsor
- Dr Vanshika Singhal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients admitted and willing for the procedure
Patients with Chronic Otitis Media Tubotympanic Type
Patients with conductive hearing loss less than 40db
Dry ear for atleast 6 weeks
Exclusion Criteria
Patients with Uncontrolled DM SHTN Bleeding Diathesis CAD
Patients with mixed hearing loss
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the graft uptake in type 1 tympanoplasty using Temporalis Fascia with PRF and with the application of PRPTimepoint: Once weekly for one month <br/ ><br>Fortnightly for three months <br/ ><br>Six months <br/ ><br> <br/ ><br>ELVE MONTHS
- Secondary Outcome Measures
Name Time Method To compare the hearing outcomes in type 1 tympanoplasty using Temporalis Fascia with PRF & with the application of PRP <br/ ><br>To assess the complications of applications of PRF & PRP in type 1 tympanoplasty <br/ ><br>Timepoint: Once weekly for one month <br/ ><br>Fortnightly for three months <br/ ><br>Six months <br/ ><br>