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Comparison of clinical outcomes between endoscopic over-underlay and overlay tympanoplasty type I for tympanic membrane perforation; Randomized clinical trial

Recruiting
Conditions
Tympanic membrane perforation, chronic otitis media
conductive hearing loss, tympanic membrane perforation
Registration Number
TCTR20230911001
Lead Sponsor
/A
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
46
Inclusion Criteria

1. Male or Female 18-75 years old, 2. Tympanic membrane perforation with dry status at least 3 months, 3. perforation size > 25%,4. Thai people

Exclusion Criteria

1. Previous tympanoplasty, 2. Tympanic membrane perforation with ossicular chain involvement ( Air-Bone gap > 30 dB, 3. Tympanic membrane perforation with cholesteatoma, 4. Tympanic membrane perforation with middle ear tumor

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Anatomic closure 6 months graft success rate
Secondary Outcome Measures
NameTimeMethod
Audiologic outcome 6 months Gap closure ,operative time in the operating room record from starting operation until end
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