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

Comparison of the efficacy of endoscopic micro-debrider assisted adenoidectomy versus conventional adenoidectomy on improvement in middle ear functions and hearing â??A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/05/008508
Enrollment
126
Registered
2017-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Patients planned for adenotonsillectomy/adenoidectomy

Interventions

Intervention1: Endoscopic microdebrider assisted adenoidectomy: Assessment of postoperative improvement in middle ear function and hearing after endoscopic microdebrider assissted adenoidectomy. Contr

Sponsors

JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Hearing improvement in decibels. Improvement in middle ear function parameters like middle ear pressure, compliance and acoustic reflex on impedance audiometryTimepoint: Pre operative, post operatively on 2nd day, 7th day, 4th week, 6th week and 12th week.

Secondary

MeasureTime frame
1. Presence of residual adenoid tissue 2. Improvement in nasal obstruction and snoring 3. Damage to adjacent structures 4.Condition of tympanic membrane(position/appearance) Timepoint: Pre operative, post operatively on 2nd day, 7th day, 4th week, 6th week and 12th week.

Countries

India

Contacts

Public ContactNikhil Rajan

JIPMER

sunil_58@rediffmail.com9442527018

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026