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Detection of Group A β-Hemolytic Streptococci in Oral Samples

H

Hero Scientific

Status

Unknown

Conditions

Group A β-Hemolytic Streptococci

Treatments

Other: Collection of oral and/or nasal samples

Study type

Observational

Funder types

Industry

Identifiers

NCT05223634
STRP.P002

Details and patient eligibility

About

This prospective, sample collection study will assess different oral and/or nasal sample types collected from patients suspected of suffering from GABHS pharyngitis to conduct research and development on innovative GABHS detection methods specific for each sample type.

Full description

Study candidates are patients age 3 and older with complaints of sore throat and are suspected of suffering from GABHS pharyngitis. Patients who consent and are found eligible will be enrolled in the study. Subjects will be tested according to the conventional standard of care in addition to providing extra specimen samples for the study.

After each patient has been tested according to conventional SOC and has enrolled in the study, up to ten oral and/or nasal specimen samples will be collected . Study participation is complete once all specimen samples are collected.

Most or all collected samples will be qualitatively tested and may also be quantitatively and/or semi-quantitatively tested for the presence of GABHS. Some collected samples may additionally or alternatively be tested for other respiratory infections as well. (such as SARS-CoV-2, influenza, etc.)

Enrollment

300 estimated patients

Sex

All

Ages

3+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patient, either male or female, is age 3 years or older;
  2. Patient is suspected of suffering from GABHS pharyngitis, and is prescribed a throat culture by conventional SOC;
  3. Patient or legal guardian is able to communicate with study personnel;
  4. Patient or legal guardian is able to understand oral and written information regarding the nature of the study and is willing to provide written informed consent.

Exclusion criteria

  1. Patients presently on antibiotics prescribed by a physician for treatment or prevention of GAS infection or has taken antibiotics within the past 3 days ( unless patient only first started taking antibiotics within the past 24 hour)
  2. pregnancy
  3. Patients who took mouth rinse or taking oral treatment for mouth sores within 3 hours of study

Trial design

300 participants in 1 patient group

oral and/or nasal specimen samples
Description:
After each patient has been tested according to conventional SOC and has enrolled in the study, up to ten oral and/or nasal specimen samples will be collected
Treatment:
Other: Collection of oral and/or nasal samples

Trial contacts and locations

1

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Central trial contact

Donna Ehrenberg; Robert Levitz

Data sourced from clinicaltrials.gov

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