A Comparative Study of the Outcomes of 2 Surgical Procedures for Safe Type of Chronic Otitis Media
Primary Purpose
Chronic Otitis Media, Tubotympanic Disease
Status
Unknown status
Phase
Phase 3
Locations
India
Study Type
Interventional
Intervention
mastoidotympanoplasty and tympanoplasty
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Otitis Media focused on measuring Otitis media suppurative, surgery ear
Eligibility Criteria
Inclusion Criteria:Chronic tubotympanic otitis media in quiescent phase with intact ossicular chain - Exclusion Criteria:1. atticoantral otitis media 2. Specific otitis media 3. Sensorineural hearing loss 4. Fixed/Dislocated ossicular chain 5. Uncorrectable disease focus in nose/throat 6. Chronic otitis media in active phase 7. Chronic otitis media with complications 8. Extensive unresectable tympanosclerosis -
Sites / Locations
- Department of ENT, KIMS
Outcomes
Primary Outcome Measures
Pure tone audiometry
Impedance audiometry
Otoendoscopy
External ear canal dimensions
Secondary Outcome Measures
Full Information
NCT ID
NCT00271778
First Posted
January 3, 2006
Last Updated
January 3, 2006
Sponsor
Karnataka Institute of Medical Sciences
1. Study Identification
Unique Protocol Identification Number
NCT00271778
Brief Title
A Comparative Study of the Outcomes of 2 Surgical Procedures for Safe Type of Chronic Otitis Media
Official Title
A Randomized Control Study of the Outcomes of Mastoidotympanoplasty Versus Tympanoplasty in Quiescent Tubotympanic Otitis Media
Study Type
Interventional
2. Study Status
Record Verification Date
December 2005
Overall Recruitment Status
Unknown status
Study Start Date
July 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Karnataka Institute of Medical Sciences
4. Oversight
5. Study Description
Brief Summary
Mastoidotympanoplasty is a recognised surgery that is performed for chronic otitis media. But whether mastoidectomy in addition to tympanoplasty is really necessary in each and every case of quiescent chronic otitis media still remains controversial. Hence this study has been undertaken to study the differences in the outcomes of the 2 surgical procedures performed for chronic otitis media in a randomized control design.
Detailed Description
Design: single blinded randomized control study. Setting: Tertiary referral medical college hospital. Sample size: 60. No of groups: 2 [30 cases in each group]. Group 1: Patients undergoing mastoidotympanoplasty. Group 2: Patients undergoing tympanoplasty only. No of strata: 3.
Outcomes:
Improvement of hearing
Closure of tympanic perforation
Recurrence of disease
external ear canal stenosis
Tools for measurement of outcomes [before and after surgery]:
Pure tone audiometry
Impedance audiometry
Otoendoscopy
External ear canal dimensions
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Otitis Media, Tubotympanic Disease
Keywords
Otitis media suppurative, surgery ear
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
60 (false)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
mastoidotympanoplasty and tympanoplasty
Primary Outcome Measure Information:
Title
Pure tone audiometry
Title
Impedance audiometry
Title
Otoendoscopy
Title
External ear canal dimensions
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:Chronic tubotympanic otitis media in quiescent phase with intact ossicular chain -
Exclusion Criteria:1. atticoantral otitis media 2. Specific otitis media 3. Sensorineural hearing loss 4. Fixed/Dislocated ossicular chain 5. Uncorrectable disease focus in nose/throat 6. Chronic otitis media in active phase 7. Chronic otitis media with complications 8. Extensive unresectable tympanosclerosis
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vikram K Bhat, MS, DNB.
Organizational Affiliation
Karnataka Institute of Medical Sciences, Hubli, India
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Khaja Naseeruddin, MS, DLO.
Organizational Affiliation
Vijayanagar Institute of Medical Sciences, Bellary, India
Official's Role
Study Director
Facility Information:
Facility Name
Department of ENT, KIMS
City
Hubli
State/Province
Karnataka
ZIP/Postal Code
580021
Country
India
12. IPD Sharing Statement
Learn more about this trial
A Comparative Study of the Outcomes of 2 Surgical Procedures for Safe Type of Chronic Otitis Media
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