- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01031082
Study to Identify and Characterize Bacteria Causing Acute Otitis Media in South African Children
May 20, 2010 updated by: GlaxoSmithKline
Identification and Characterization of the Bacteria Causing Acute Otitis Media (AOM) Episodes in HIV-positive and HIV-negative Children in South Africa
The purpose of this study is to identify and characterize the bacteria causing acute otitis media episode in HIV-positive and HIV-negative children (>=3 months to <5 years) in South Africa.
Middle ear fluid sampling either by tympanocentesis or by careful sampling of spontaneous otorrhoea will be done; nasopharyngeal aspirate and urine sample will also be collected from the subjects.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
265
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Gauteng
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Soweto, Gauteng, South Africa, 2013
- GSK Investigational Site
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 months to 5 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Children aged >= 3 months and < 5 years seeking healthcare for the treatment of acute otitis media.
Description
Inclusion Criteria:
Inclusion criteria for all subjects:
- Age: >= 3 months and < 5 years at the time of enrolment.
- 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.
- Subject will be included as a treatment failure case.
- Written informed consent obtained from parent or guardian prior to study start.
Inclusion criteria for HIV-positive subjects:
- Documented HIV-positive status as given in subject's medical records. or
- Subjects referred from paediatric HIV clinic.
Inclusion criteria for HIV-negative subjects (including presumed negative children)
- Children who have been tested HIV-negative.
- Children whose mothers volunteer to have tested HIV-negative whilst pregnant with the index case and the child is free to any World Health Organization Grade II stigmata of HIV/acquired immunodeficiency syndrome.
- Children who do not fulfil the World Health Organization staging for HIV infection / immunosuppression.
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 but excluding cotrimoxazole or isoniazid prophylaxis in HIV exposed children.
- Provision of antibiotic by paediatrician/ENT specialist at the enrolment visit prior to the sampling of the middle ear fluid or spontaneous Otorrhoea.
- Children on antibiotics for acute otitis media who are clinically improving.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
HIV-negative Group
This group is sub-divided into two sub-groups.
One sub-group includes HIV-negative/ presumed negative subjects with a new episode of acute otitis media who have not yet received antibiotic therapy for the episode and the other sub-group includes HIV-negative/ presumed negative subjects with treatment failure who have had a diagnosis of acute otitis media and showed no clinical improvement within 48-72 hours of antibiotic treatment.
|
Middle ear fluid, nasopharyngeal aspirate and urine sample collection.
|
|
HIV-positive Group
This group is sub-divided into two sub-groups.
One sub-group includes HIV-positive subjects with a new episode of acute otitis media who have not yet received antibiotic therapy for the episode and the other sub-group includes HIV-positive subjects with treatment failure who have had a diagnosis of acute otitis media and showed no clinical improvement within 48-72 hours of antibiotic treatment.
|
Middle ear fluid, nasopharyngeal aspirate and urine sample collection.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
|---|
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Occurrence of bacterial pathogens isolated from middle ear fluid samples in HIV-positive and HIV-negative subjects.
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Secondary Outcome Measures
Outcome Measure |
|---|
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Occurrence of bacterial serotypes.
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Antimicrobial susceptibility of different bacteria isolated from middle ear fluid samples as assessed by standard microbiological techniques.
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Occurrence of treatment failure of acute otitis media and of recurrent acute otitis media.
|
|
Occurrence of spontaneous otorrhoea.
|
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Occurrence of bacteria in acute otitis media cases with treatment failure and in new acute otitis media cases without treatment therapy.
|
|
Occurrence of bacteria in acute otitis media cases vaccinated with a pneumococcal vaccine.
|
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Frequency of concurrent respiratory viral infection coinciding with the episode of acute otitis media.
|
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The comparison of above endpoints in HIV-positive and HIV-negative subjects.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2009
Primary Completion (Actual)
May 1, 2010
Study Completion (Actual)
May 1, 2010
Study Registration Dates
First Submitted
December 10, 2009
First Submitted That Met QC Criteria
December 10, 2009
First Posted (Estimate)
December 14, 2009
Study Record Updates
Last Update Posted (Estimate)
May 24, 2010
Last Update Submitted That Met QC Criteria
May 20, 2010
Last Verified
May 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 112135
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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