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effect of replacing the diseased small bones in the ear with bow shaped cartilage from ear on hearing

Not Applicable
Conditions
Health Condition 1: null- chronic suppurative otitis media- atticoantral disease
Registration Number
CTRI/2017/09/009798
Lead Sponsor
Jawaharlal Institute of Postgraduate Medical Education and Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Adult patients with chronic otitis media undergoing type III tympanoplasty who are diagnosed to be having an absence of the stapes supra-structure during surgery will be considered for this procedure.

Exclusion Criteria

1.Patients in whom stapes footplate is fixed or obliterated

2.Patients in whom facial nerve is dehiscent and bulging over the stapes footplate.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hearing loss in decibels at 250, 500, 1000, 2000 and 4000 Hz preoperatively and postoperatively at 12 weeksTimepoint: 12 weeks
Secondary Outcome Measures
NameTimeMethod
incidence of intraoperative and postoperative complicationsTimepoint: 12 weeks
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