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Respiferon Project

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Enrolling

Conditions

Respiratory Viral Infection

Treatments

Diagnostic Test: Evaluate the performance of IFN I/III

Study type

Observational

Funder types

Other

Identifiers

NCT06017310
69HCL23_0697

Details and patient eligibility

About

Respiratory viral infections (RVIs) represent a major public health problem and a great burden in terms of morbidity and mortality in children and adults worldwide. To ascertain the source of an infection, microbiology laboratories routinely perform a crucial step: the search for the pathogen through Polymerase Chain Reaction (PCR). Due to the extensive variety of pathogens, testing for the existence of all potential viruses, bacteria, or fungi accountable for the infection is an impractical and time-intensive endeavor. Furthermore, the rise of novel pathogens, exemplified by those accountable for the recent SARS-CoV-2 pandemic, underscores the urgency of promptly developing new innovative diagnostic tests.

To address these needs, researchers have dedicated several years to developing indirect methodologies notably centered around utilizing markers derived from the host's immune system. Among these, one particularly promising approach focuses on measuring the expression of interferon-stimulated genes, which are uniquely triggered by viral infections, thereby facilitating viral diagnosis. This methodology's efficacy has been proven in the context of SARS-CoV-2 infections.

This study's objective is to assess the functionality of such a tool across a spectrum of Respiratory Viral Infections (RVIs) prevalent within a French population during the winter season.

Enrollment

1,000 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Positive nasopharyngeal samples for the detection of a virus, for which the replicative character has been established by the viral culture technique (500µL minimum required)
  • Samples kept at the CRB since 2018
  • Information to patients carried out and non-objection collected-

Exclusion criteria

  • N/A

Trial design

1,000 participants in 2 patient groups

Replicative viruses
Description:
Presence of a replicative virus determined by viral culture
Treatment:
Diagnostic Test: Evaluate the performance of IFN I/III
Unreplicative viruses
Description:
Absence of a replicative virus determined by viral culture
Treatment:
Diagnostic Test: Evaluate the performance of IFN I/III

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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