Comparison of The Efficacy of Endoscopic versus Microscopic Myringoplasty(surgical techniques) in Management of ear drum Perforations: A Randomized Clinical Trial.

Recruiting

Conditions: chronic suppurative otitis media tubotympanic type

Registration Number: CTRI/2017/08/009199

Lead Sponsor: Jawaharlal Institute of Postgraduate Medical Education and Research

Brief Summary: Comparision of the efficacy of endoscopic versus Microscopic Myringoplasty in the management of pars tensa perforations : A Randomised clinical trial.

Closure of tympanic membrane perforations in the pars tensa region in a case of CSOM tubo tympanic type disease is known as myringoplasty. Various advancements in this surgery are now available and here we compare 2 novel procedures done for the treatment of pars tensa perforations. Hearing outcomes after both types of surgery will be assessed as the primary outcome and graft uptake will be the secondary outcome of this study. Block randomization will be followed. Data collection will be done and patient will be followed up post operatively at 8 weeks and 3 months for hearing assessment and graft uptake.Unpaired t test will be used to compare hearing outcomes between both the groups.Graft uptake will be statistically assessed by the chi square test or fischers test. This study aims to show both the techniques used for pars tensa perforation repair and advantages and disadvantages of each.

Detailed Description: Not available

Recruitment & Eligibility

Status: Open to Recruitment

Sex: All

Target Recruitment: 108

Inclusion Criteria

All diagnosed cases of CSOM TTD with pars tensa perforation and conductive hearing loss in the age group of 18 to 50 years of both sex in JIPMER hospital.

Exclusion Criteria

Patients with active discharge from middle ear 2 CSOM of attico antral type 3.
Patients with otitis externa 4.
Patients with sensorineural hearing loss or mixed type hearing loss 5 Patients with abnormalities in ossicular chain 6 Patients with nasal allergy, bleeding diathesis, diabetes, hypertension.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare hearing outcome in both the groups in the treatment of CSOM TTD	Pre operative \| 8 weeks \| 3 months

Secondary Outcome Measures

Name	Time	Method
To compare graft uptake between both the groups	8 weeks

Trial Locations

Locations (1): JIPMER
🇮🇳
Pondicherry, PONDICHERRY, India
JIPMER
🇮🇳Pondicherry, PONDICHERRY, India
R Chandra Shekar Reddy
Principal investigator
9989303942
dr.rcsreddy91@gmail.com