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Methods of Assessment of Adenoid Size

A

Assiut University

Status

Unknown

Conditions

Adenoid Hypertrophy

Treatments

Procedure: flexible nasoendoscopy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Chronic nasal obstruction due to adenoid hypertrophy is among the most common health problems affecting children, and adenoidectomy is one of the most common surgical procedures performed in this age group Because of difficulties associated with the use of the objective methods (such as nasopharyngeal endoscopy) in young children, the development of a reliable scale based on the child's symptoms to properly evaluate the need for surgical intervention would be of great value for clinicians. When adenoidectomy is being considered, the diagnosis and documentation of adenoidal hypertrophy become an important issue. Numerous modalities have been used for this task, including trans oral digital palpation and trans oral mirror examination; however, these methods are quite impractical with uncooperative younger children

Full description

Assessment of the nasopharynx and adenoids by fibreoptic examination bears the advantage of direct visualization of the postnasal space. In addition, previous studies have demonstrated that adenoid size, as determined by rhinoscopy, was well correlated with clinical symptoms such as nasal obstruction and snoring.

The aim of this study was to compare the effectiveness of lateral neck radiography and video rhinoscopy in assessing adenoid size .

Assessment of the reproducability of these modalities to associated symptoms and, thus, the severity of the disease.

Enrollment

100 estimated patients

Sex

All

Ages

3 to 14 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • children aged 3 _ 14 years old
  • clinical diagnosis of adenoid hypertrophy in the form of chronic oral respiration , nasal disorders and snoring
  • recurrent otitis media

Exclusion criteria

  1. patients diagnosed with nasal obstruction due to anatomic malformation ( congenital, choanal atresia, stenosis or septal deviation )
  2. age less than 3 years or more than 14 years
  3. patient with craniofacial malformation and down syndrome

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

patients will undergo flexible nasoendoscopy
Experimental group
Description:
Endoscopy will be performed by passing the endoscope along either the floor of the nose or just under the middle turbinate. the condition of the nasal mucosa\\ septum\\ turbinates and the presence of discharge The postnasal space will be assessed . All abnormalities will be recorded .the images will be recorded and assessed separately by two independent otolaryngologists
Treatment:
Procedure: flexible nasoendoscopy

Trial contacts and locations

0

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Central trial contact

Mohamed E Abdullah, MD; ghada M Saad, MBBCH

Data sourced from clinicaltrials.gov

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