A Study to assess role of Nitrous Oxide Anaesthesia on graft uptake in Tympanoplasty surgery in children.
Not Applicable
- Conditions
- Health Condition 1: H720- Central perforation of tympanic membraneHealth Condition 2: H661- Chronic tubotympanic suppurative otitis media
- Registration Number
- CTRI/2020/05/025003
- Lead Sponsor
- ady Hardinge Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients having Chronic Suppurative Otitis Media mucosal disease both unilateral and bilateral will be included.
2. Patients having perforation in pars tensa for a minimum period of three months.
3.Patients having a dry ear period of four weeks.
Exclusion Criteria
1.Patients with Cholesteatoma in the ear.
2.Patients with granulation tissue in the ear
3.Patients with previously operated ear.
4.Patients with only one hearing ear.
5.Patients with hearing loss out of proportion to the size of perforation.
6.Patients with any congenital anomalies like cleft lip, cleft palate and syndromal diagnosis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Graft uptake success rate in paediatric tympanoplasty with and without N2O anaesthesiaTimepoint: 3 months postoperatively
- Secondary Outcome Measures
Name Time Method Audiological Success rate in Paediatric Tympanoplasty with and without N2O anaesthesia <br/ ><br>Timepoint: 3 months postoperatively;Correlation of graft uptake with Eustachian Tube functionTimepoint: 3 months postoperatively