Study to Identify and Characterize Bacteria Causing Acute Otitis Media in Young Children in Turkey

NCT ID: NCT01031329

Last Updated: 2015-04-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2012-11-30

Study Completion Date

2014-02-28

Brief Summary

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The purpose of this study is to identify and characterize the bacteria causing complicated Acute Otitis Media episode in children \>= 3 months to \< 5 years in Turkey.

Detailed Description

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Conditions

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Infections, Streptococcal

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Complicated Acute otitis media Group

This group was divided into 3 sub-groups.

* One sub-group includes treatment failure subjects who have had a diagnosis of acute otitis media and showed no clinical improvement within 48-72 hours of antibiotic treatment or reappearance of symptoms within 10 days following the end of antibiotic treatment.
* The second sub-group includes subjects with recurrent acute otitis media, who have had new episodes of acute otitis media within the past 6 months or the fourth (or greater) new episode within the past year.
* The third sub-group includes subjects with spontaneous otorrhoea if perforation has occurred \< 24 hours prior to the visit.

Tympanocenthesis and urine collection

Intervention Type PROCEDURE

Fluid using needle aspiration is obtained from middle ear fluid. Urine is collected using a urine bag.

Interventions

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Tympanocenthesis and urine collection

Fluid using needle aspiration is obtained from middle ear fluid. Urine is collected using a urine bag.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Age: \>= 3 months and \< 5 years at the time they are seen by the paediatrician. The subject becomes ineligible on the fifth birthday.
* Signs, symptoms, and conditions:
* One of the functional or general signs of otalgia ,conjunctivitis, fever and either
* Paradise's criteria or
* Spontaneous otorrhoea of less than 24 hours.
* Subjects if classified as recurrent acute otitis media or treatment failure as described below:
* Recurrent acute otitis media: Defined as a subject who has an episode of acute otitis media representing the third new episode within the past 6 months, or the fourth new episode within the past year.
* Treatment failure: Defined as a subject who was diagnosed with acute otitis media and received antibiotic treatment from a physician, but is still symptomatic 48-72 hours after initiation of the treatment. As with other acute otitis media cases, the onset of signs or symptoms should have been within 72 hours prior to the initial visit to the physician.
* Written informed consent obtained from parent or guardian prior to study start.

Exclusion Criteria

* Hospitalised during the diagnosis of acute otitis media or during treatment.
* Otitis externa, or otitis media with effusion.
* Presence of a transtympanic aerator.
* Systemic antibiotic treatment received for a disease other than acute otitis media in the 72 hours prior to enrolment.
* Receiving antimicrobial prophylaxis for recurrent acute otitis media.
* Provision of antibiotic by paediatrician at the enrolment visit prior to the sampling of the middle ear fluid or spontaneous otorrhoea.
* Patients that are on antibiotics for acute otitis media, and are clinically improving.
Minimum Eligible Age

3 Months

Maximum Eligible Age

5 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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GlaxoSmithKline

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Locations

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GSK Investigational Site

Adana, , Turkey (Türkiye)

Site Status

GSK Investigational Site

Adana, , Turkey (Türkiye)

Site Status

GSK Investigational Site

Ankara, , Turkey (Türkiye)

Site Status

GSK Investigational Site

Ankara, , Turkey (Türkiye)

Site Status

GSK Investigational Site

Istanbul, , Turkey (Türkiye)

Site Status

GSK Investigational Site

Istanbul, , Turkey (Türkiye)

Site Status

GSK Investigational Site

Izmir, , Turkey (Türkiye)

Site Status

GSK Investigational Site

Izmir, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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111339

Identifier Type: -

Identifier Source: org_study_id

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