NCT07411261Not yet recruiting
PremaBiom: Metatranscriptomics of the Respiratory Microbiome to Predict the Occurrence of Bronchopulmonary Dysplasia in Preterm Infants
Source: ClinicalTrials.gov · Last updated 13 Feb 2026
Brief summary (registry, in English)
The goal of this clinical trial is to understand the impact of respiratory microbiome maturation in respiratory health of preterm infants under 32 gestational weeks. The main questions it aims to answer are: * What is the role of microbiome maturation in respiratory health (development of bronchopulmonary dysplasia, childhood asthma and viral respiratory infections) of preterm infants ? * Which environmental or health factors are involved in the maturation of the respiratory microbiome ? Participants will undergo follow-up from birth until 3 years of corrected age including nasal swabs, stool samples, and for some of them blood and milk sample.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 270 (estimated)
- First submitted
- 4 Feb 2026
- Start date
- Mar 2026
- Primary completion date
- Mar 2029
- Lead sponsor
- University Hospital, Caen
- Diseases
- Asthma
- NCT number
- NCT07411261
What you commit to
- Study type: Interventional
- Planned participants: 270
- From Mar 2026 to the primary completion date, Mar 2029
- 6 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Palliative care only
- Lack of parental consent
- Parents who are minors or under legal protection (guardianship, conservatorship, judicial protection)
- Parents who do not speak French
Who the study is looking for
- Preterm infants with gestational age at birth lower than 32 gestational weeks and 6 days.
- Hospital stay in one of the participant neonatal care units
- Infants covered by the social security system of at least one of their parents
- Whose parents have been informed about the study and agree to sign the informed consent form
Age in the registry: - to 72 hours · Sex: All · Does not accept healthy volunteers
Sites (6)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Service de néonatalogie, CHU d'Amiens Coordinator of this site? Confirm its status | Amiens | France | Unknown status |
| Service de néonatalogie, CHU de Caen Coordinator of this site? Confirm its status | Caen | France | Unknown status |
| Service de néonatalogie, CH Cherbourg-en-Cotentin Coordinator of this site? Confirm its status | Cherbourg | France | Unknown status |
| Service de néonatalogie, GHT du Havre Coordinator of this site? Confirm its status | Le Havre | France | Unknown status |
| Service de néonatalogie, CHRU de Lille Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| Service de néonatalogie, CHU de Rouen Coordinator of this site? Confirm its status | Rouen | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.