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Study to Identify and Characterize the Bacteria Causing Acute Otitis Media Episodes in Young Children in Saudi Arabia

Identification and Characterization of the Bacteria Causing Acute Otitis Media (AOM) Episodes in Young Children in Saudi Arabia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01204385
Enrollment
66
Registered
2010-09-17
Start date
2009-06-30
Completion date
2011-05-31
Last updated
2014-01-13

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

Conditions

Infections, Streptococcal

Keywords

Non-typeable Haemophilus Influenzae, Acute Otitis Media, Streptococcus Pneumoniae, etiology

Brief summary

The purpose of the study is to identify the bacterial aetiology of acute otitis media episodes in young children aged ≥ 3 months to \< 5 years in Saudi Arabia.

Interventions

PROCEDURESample collection

Middle ear fluid and urine

Sponsors

GlaxoSmithKline
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Months to 5 Years
Healthy volunteers
No

Inclusion criteria

A child will be eligible for inclusion if he/she meets the following criteria: * Age: ≥ 3 months and \< 5 years at the time of enrolment. The subject becomes ineligible on the fifth birthday. * Signs, symptoms, and conditions: i. One of the functional or general signs of otalgia (or its equivalent: irritability), conjunctivitis, fever AND EITHER ii. Paradise's criteria (bulging, diffused or localised inflamed tympanic membranes) OR iii. Spontaneous otorrhoea of less than 24 hours * Onset of signs and symptoms of AOM within 72 hours prior to diagnosis of AOM by a physician. To be included as treatment failure, subjects must have then received antibiotic treatment from the physician, but remain symptomatic 48-72h after initiation of treatment * Written informed consent obtained from parent or guardian prior to study start.

Exclusion criteria

The following criteria should be checked at the time of study entry. If any apply, the child must not be included in the study. * Hospitalised during the diagnosis of AOM or during treatment, * Otitis externa, or otitis media with effusion * Presence of a transtympanic aerator * Systemic antibiotic treatment received for a disease other than AOM in the 72 hours prior to enrolment, * Receiving antimicrobial prophylaxis for recurrent AOM, * Provision of antibiotic by paediatrician/ENT specialist at the enrolment visit, prior to the sampling * Patients on antibiotics for AOM who are clinically improving.

Design outcomes

Primary

MeasureTime frame
Occurrence of H. influenzae, S. pneumoniae and other bacterial pathogens isolated from middle ear fluid samplesAverage time frame: 12 months

Secondary

MeasureTime frame
Antimicrobial susceptibility of H. influenzae, S. pneumoniae and Moraxella catarrhalis isolated from middle ear fluid samples as assessed by standard microbiological techniquesAverage time frame: 12 months
Occurrence of treatment failure of acute otitis media and of recurrent acute otitis media (≥ 3 episodes in the last 6 months or ≥ 4 episodes in 12 months)Average time frame: 12 months
Occurence of H. influenzae and S. pneumoniae serotypesAverage time frame: 12 months
Occurrence of H. influenzae in acute otitis media cases with treatment failure and in new acute otitis media cases without treatment therapyAverage time frame: 12 months
Occurrence of H. influenzae in acute otitis media cases vaccinated with a pneumococcal vaccineAverage time frame: 12 months
Occurrence of spontaneous otorrheaAverage time frame: 12 months

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026