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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

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Service de néonatalogie, CHU d'Amiens
Coordinator of this site? Confirm its status
AmiensFranceUnknown status
Service de néonatalogie, CHU de Caen
Coordinator of this site? Confirm its status
CaenFranceUnknown status
Service de néonatalogie, CH Cherbourg-en-Cotentin
Coordinator of this site? Confirm its status
CherbourgFranceUnknown status
Service de néonatalogie, GHT du Havre
Coordinator of this site? Confirm its status
Le HavreFranceUnknown status
Service de néonatalogie, CHRU de Lille
Coordinator of this site? Confirm its status
LilleFranceUnknown status
Service de néonatalogie, CHU de Rouen
Coordinator of this site? Confirm its status
RouenFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.