Actively Recruiting

Age: 2Years - 5Years
All Genders
ID06998264

In-depth Analysis of the Immune Responses in the Upper Respiratory Tract of Influenza-infected Children

Led by University Hospital, Geneva · Updated on 2025-05-31

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the immune response in the upper respiratory tract of children aged 2 to 5 who have a laboratory-confirmed influenza infection. This observational study aims to measure inflammation in the nasal cavity, relate it to viral load and clinical symptoms, and compare it with responses in the blood. The project also includes comparison to children without infection or those vaccinated with a nasal flu vaccine in a related study. Participants will have two main study visits: the first within 72 hours of hospital admission and the second about one month later. During these visits, samples of blood, nasal lining fluid, nasal cells, and saliva will be collected. Nasal lining fluid and saliva samples will also be taken every two to three days until symptoms resolve. Symptom-related questions will be asked during these visits. Throughout the study, researchers will assess inflammatory markers like pro-inflammatory cytokines in nasal fluid, immune cell types in nasal and blood samples, influenza-specific antibodies, and viral load in nasal and saliva samples. Clinical symptoms and outcomes such as fever duration, oxygen use, secondary infections, intensive care stays, and rehospitalization will be recorded. The total study participation lasts about one month from initial hospitalization.

CONDITIONS

Brief Title

In-depth Analysis of the Immune Responses in the Upper Respiratory Tract of Influenza-infected Children

Who Can Participate

Age: 2Years - 5Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 2 to 5 years
  • Presenting clinical signs of an influenza-like illness
  • Having a positive laboratory test for influenza at the same time
Not Eligible

You will not qualify if you...

  • Immunosuppression
  • Intubation or under invasive mechanical ventilation
  • Co-infection with RSV or SARS-CoV-2

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 1 month

Participants are observed to analyze immune responses and clinical outcomes related to influenza infection.

1 baseline visit and periodic assessments during hospitalization

Trial Site Locations

Total: 1 location

1

Geneva University Hospitals

Geneva, Switzerland, 1205

Actively Recruiting

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Research Team

J

Jennifer Villers, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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