It is Accepted That Adenoid Hypertrophy is Related to Otitis Media With Effusion Incidence. Better Understanding of the Correlation Between the Relative Size of AH and the Incidence of Persistent OME May Provide Evidence to Support a More Standardized Approach to the Diagnosis and Treatment of OME.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-16
SponsorAssiut University

About this trial

The aim of this study is to further investigate the correlation between Site and size of adenoid hypertrophy and middle ear effusion in order to provide evidence for designing a more standardized approach to the diagnosis and treatment of OME.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Children (until age of 16 years old).

Patients with adenoid hypertrophy.

Patients with OME.

Disqualifiers

Children known to have cleft palate, submucous cleft palate or other medical problems causing velopharyngeal insufficiency.

Down's syndrome, septal deviation, primary ciliary dyskinesia (Kartagener's syndrome), previous head or ear trauma, or previous myringotomy with ventilation tube insertion

Systemic medical problems interfering with surgery.

Refusal of parents to participate.

Trial population

Children age group (from 1 year old till 16 years old), male and female are included, with symptoms and signs of adenoid hypertrophy

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Comparing presence of middle ear effusion in relation to site and size of adenoid hypertrophy

The incidence of OME with each AH grade occurring in each age group of the sample size.

Time frame
Baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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