Actively Recruiting

Age: 60Years - 85Years
All Genders
Healthy Volunteers
ID06998251

In-depth Analysis of Immune Responses in the Upper Respiratory Tract in Older Adults Infected or Colonized With Streptococcus Pneumoniae (Spn)

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

280

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand the immune response in the upper respiratory tract of adults aged 60 to 85 who have pneumonia caused by Streptococcus pneumoniae (Spn) infection. It compares the immune reaction during the acute infection phase and recovery to that in people who carry Spn without symptoms and patients with confirmed viral respiratory infections like flu or respiratory syncytial virus (RSV). The study focuses on measuring inflammation in the nose and correlating it with bacterial or viral load and clinical signs, also comparing nasal and blood immune responses. Participants fall into one of three groups: hospitalized patients with confirmed Spn pneumonia, those hospitalized with flu or RSV infection, and healthy individuals carrying Spn without symptoms. Each participant will have two main visits: one within 72 hours of hospital admission and another one month later. During these visits, blood samples, nasal lining fluid, nasal cells, and saliva are collected. Nasal fluid and saliva samples are also taken every two to three days until hospital discharge or symptom resolution. Throughout the study, symptom questionnaires are completed, and various immune markers are measured including pro-inflammatory cytokines in nasal fluid, immune cell types in nasal and blood samples, antibody levels, and bacterial or viral load. Clinical outcomes like pneumonia diagnosis, severity scores, symptom severity, fever days, oxygen use, complications, ICU transfers, length of stay, mechanical ventilation, rehospitalization, and medication prescriptions are tracked for one month. The study period continues until one month after hospital admission or symptom resolution.

CONDITIONS

Brief Title

In-depth Analysis of the Immune Responses in the Upper Respiratory Tract in Older Adults Infected or Colonized With Streptococcus Pneumoniae (Spn)

Who Can Participate

Age: 60Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 60 to 85 years
  • Able to provide informed consent independently or via legal representative
  • Group 1: Clinical and/or radiological signs of pneumonia
  • Group 1: Positive Spn urinary antigen and/or blood culture and/or sputum test
  • Group 2: Clinical signs of respiratory infection
  • Group 2: Positive test for influenza or RSV
  • Group 3: Healthy without infection symptoms or lower respiratory symptoms in the past month
Not Eligible

You will not qualify if you...

  • Immunosuppression
  • Use of inhalation and/or nasal steroids in the last month
  • Currently intubated or on invasive mechanical ventilation
  • Long-term antibiotic treatment prior to disease onset

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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)

Diagnostic Evaluation

Duration - Up to 1 month

Participants undergo diagnostic testing to confirm infection or colonization status and to assess clinical signs and symptoms.

1 to 2 visits depending on participant group

Long-term Monitoring

Duration - 1 month

Participants are monitored for immune response markers, bacterial and viral load, and clinical outcomes over one month.

Multiple visits over 1 month for sample collection and assessments

Trial Site Locations

Total: 1 location

1

Geneva University Hospitals

Geneva, Switzerland, 1205

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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

3

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