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Rapid Strep Testing in Children With Recent Streptococcal Pharyngitis

Rapid Strep Testing in Children With Recent Streptococcal Pharyngitis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03055728
Enrollment
600
Registered
2017-02-16
Start date
2013-05-09
Completion date
2018-01-16
Last updated
2018-06-07

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

Conditions

Streptococcal Infections

Keywords

streptococcal infections, rapid strep testing, rapid antigen detection test

Brief summary

The purpose of this study is to determine if the rapid antigen detection test for Group A streptococcal pharyngitis diagnosis might yield higher rates of false positive results in patients who have been treated for GAS pharyngitis within 28 days of the test.

Detailed description

Strep pharyngitis, or strep throat, is a common infection afflicting children, aged 2 and above. Testing for strep pharyngitis consists of a rapid test and/or a throat culture. However, it has been observed that rapid testing may not be accurate in children with a recent history of strep pharyngitis. Therefore, this study aims to determine the accuracy of rapid strep testing in children who are presenting with symptoms of strep throat, who also have a recent history of and treatment for strep pharyngitis. By demonstrating an inaccuracy in rapid strep testing in patients with a recent history of strep pharyngitis, unnecessary testing and antibiotic use may be decreased, thereby reducing costs, overuse of antibiotics, and antibiotic resistance. The participants in the study will include 600 children, aged 2 to 20 years old, selected from a private practice in Northern Virginia who present to the practice with signs or symptoms suggestive of acute pharyngitis. Subjects are children who are presenting with signs and symptoms suggestive of acute pharyngitis by the Centor criteria, including sore throat, fever, abdominal pain and cervical lymphadenitis. Any child with above presenting symptoms who is to undergo Streptococcus rapid antigen testing will be recruited to participate in the study. A letter of consent will be provided to the parents and guardians of the involved child, stating that the study will be voluntary and confidential, and that all results will be kept in a safe environment. Investigators will be testing the difference between two proportions, the false positive rate in previously treated compared to those not treated.

Interventions

DIAGNOSTIC_TESTRapid strep antigen detection test

Pharyngeal swab for rapid antigen detection of streptococcus

DIAGNOSTIC_TESTthroat culture

Pharyngeal swab for culture for bacteria (specifically streptococcus) presence

Sponsors

Georgetown University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
2 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

* 2-20 years old * Current signs and symptoms suggestive of acute pharyngitis, including sore throat, fever, abdominal pain and cervical lymphadenitis.

Exclusion criteria

* Potential subjects who have been treated with less than 10 days of antibiotic therapy * Patients who report non-compliance with previous antibiotic therapy * Patients who have already been included in the study and children with evidence of GAS carrier status

Design outcomes

Primary

MeasureTime frameDescription
Rate of false positives and false negatives in rapid antigen testing compared to throat culture48-72 hoursThe primary objective is to use rapid antigen test results to compare the sensitivity and specificity of rapid antigen testing in children with symptoms of pharyngitis with and without a recent history of Group A streptococcus pharyngitis.

Countries

United States

Outcome results

None listed

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