Bronchial Epithelium of Children With Post-infectious Bronchiolitis Obliterans
Launched by INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE, FRANCE · Nov 14, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a condition called bronchiolitis obliterans (BO), which can happen in children after a serious lung infection, often caused by viruses like adenovirus or rhinovirus. The goal of the study is to look at the nasal lining of young children to understand how it might change in those who go on to develop BO. Researchers want to find out if there are differences in the nasal cells of children who have viral infections and later develop BO compared to those who do not.
Eligible participants are children aged 1 month to 6 years who have been hospitalized with a confirmed adenovirus or rhinovirus infection. Parents will need to read, understand, and sign a consent form for their child to participate. During the study, children will have nasal samples taken, and if they develop BO, additional tests will be done to gather more information about their condition. This research aims to help improve our understanding of bronchiolitis obliterans and eventually lead to better treatments for affected children.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Children from 1 month to 6 years hospitalized at the Timone Enfant University Hospital
- • 2. Diagnosis of an adenovirus or rhinovirus respiratory infection confirmed on a nasal swab, made upon arrival as part of the child's initial care
- • 3. Consent form read, understood, approved and signed by parents before any study procedure
- • 4. Affiliation to a social security scheme or beneficiary of such a scheme
- The inclusion criteria for children who were not hospitalized when diagnosed with an adenovirus and rhinovirus respiratory infection at the Timone Enfant University Hospital are:
- • 1. Children from 1 month to 6 years old transferred to the Timone Enfant University Hospital
- 2. Show the following signs:
- • has. Clinical: clinical signs persist 6 weeks after a viral infection: tachypnea, wheezing and/or persistent hypoxemia b. Scan: mosaic appearance +/- bronchiectasis, atelectasis vs. +/- EFR if performed: obstructive ventilatory disorder not or only slightly reversible after bronchodilators
- • 3. Consent form read, understood, approved and signed by parents before any study procedure
- • 4. Affiliation to a social security scheme or beneficiary of such a scheme
- Exclusion Criteria:
- • 1. Refusal of participation in the study by the family will be a reason for non-inclusion, as well as in the absence of parental authority.
- • 2. The existence of an underlying chronic pulmonary pathology (e.g. cystic fibrosis, ciliary dyskinesia).
- • 3. A coagulation pathology.
About Institut National De La Santé Et De La Recherche Médicale, France
The Institut National de la Santé et de la Recherche Médicale (INSERM) is France's key public research organization dedicated to advancing knowledge in health and biomedical sciences. Established to foster innovation and improve public health outcomes, INSERM conducts a wide range of clinical trials and research initiatives aimed at translating scientific discoveries into effective medical treatments and interventions. With a focus on collaboration among researchers, healthcare professionals, and industry partners, INSERM plays a pivotal role in shaping health policies and enhancing the quality of care in France and beyond.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Marseille, , France
Patients applied
Trial Officials
Julie MAZENQ, PhD
Principal Investigator
APHP Marseille
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported