Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
Actively Recruiting
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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