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Comparison of efficacy of two surgical methods for nasal blockade due to adenoids

Not Applicable
Conditions
Health Condition 1: null- Patients planned for adenotonsillectomy/adenoidectomy
Registration Number
CTRI/2017/05/008508
Lead Sponsor
JIPMER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
126
Inclusion Criteria

All diagnosed cases of symptomatic adenoid hypertrophy with middle ear dysfunction or effusion and/or hearing impairment between 5 to 16 years of age, of both the genders, undergoing adenoidectomy or adenotonsillectomy in JIPMER during the study period.

Exclusion Criteria

1) history of previous adenotonsillectomy

2) significant deviated nasal septum

3) co-existent cleft palate or sub-mucous cleft palate

4) active upper respiratory infection

5) other causes of conductive hearing loss like CSOM

6) bleeding disorders

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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