Actively Recruiting
Association of Dysbiosis and Immune Response in Bronchiolitis in Infants Under 12 Months
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-02-26
120
Participants Needed
3
Research Sites
4 weeks
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
I
Infectious Diseases Models for Innovative Therapies center
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying acute bronchiolitis, a common lung infection in children under two years old caused mainly by the respiratory syncytial virus (RSV). The study aims to understand why it is difficult to predict how severe the infection will become by looking at the role of the microbiota (gut, oral, and nasal bacteria) and the immune response to RSV in affected children. This observational study includes infants under 12 months old with bronchiolitis during the RSV season. The study involves collecting samples from 80 infants with different severities of bronchiolitis, including hospitalized, non-hospitalized, and those in intensive care. Researchers will take oral, nasal, and stool samples to study the microbiota and will collect capillary or venous blood samples to analyze immune responses. These samples help identify bacterial imbalances and immune markers during infection. Participants will provide these samples once during their illness. Researchers will measure dysbiosis, immune system markers like cytokines and chemokines, viral genetics, RSV antibodies, and bacterial load. The study team monitors these factors to better understand infection severity and immune response. The study runs from December 2024 through April 2026, and participation involves only sample collection with no treatment interventions.
CONDITIONS
Brief Title
Association of Dysbiosis and Immune Response in Bronchiolitis in Under 12 Months -Old Infants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Infants younger than 12 months
- Bronchiolitis during the RSV epidemic season
- No chronic illness
- No previous history of bronchiolitis
- Signed consent from parents or legal guardians
You will not qualify if you...
- Chronic respiratory illness
- History of bronchiolitis or newborn asthma
- Treatment with immunosuppressants
- No social security affiliation
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 - 1 day
Participants undergo single-time sampling including blood samples and swabs to study dysbiosis and immune response during bronchiolitis.
1 visit (in-person)
Trial Site Locations
Total: 3 locations
1
APHP, Antoine Béclère Hospital
Clamart, France, 92140
Actively Recruiting
2
AP-HP,Raymond Poincaré Hospital
Garches, France, 92380
Actively Recruiting
3
Réanimation médico-chirurgicale Necker
Paris, France, 750
Actively Recruiting
Research Team
E
Etienne BIZOT, Doctor
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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