Clinical trial Recruiting at 1 site Observational Ages 0 Days to 3 Days

Investigating biomarkers for early prediction of bronchopulmonary dysplasia in preterm infants

Official title: The Role of Volatile Organic Compounds (VOCs), Airway Mucins and Microbiome in the Development of Bronchopulmonary Dysplasia and the Feasibility of Exhaled Breath VOCs Analysis as an Early Detection Tool

Run by University Hospital, Antwerp · NCT06342752 · Data updated 2026-11-12

This study is trying to find early signs that can help predict if premature babies will develop bronchopulmonary dysplasia, using samples from their breath, throat, and placenta.

More Bronchopulmonary Dysplasia trials

Quick facts

Study typeObservational
Ages0 Days to 3 Days
SexAll
Enrollment140 (estimated)
SponsorUniversity Hospital, Antwerp
Academic / other
Locations1 site (Edegem, Antwerp)
StatusRecruiting
StartedJune 14, 2024
Main results expectedSeptember 2026
Study endsSeptember 2027
Registry record updatedMay 9, 2025
Trial IDNCT06342752 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are infants born at a gestational age of less than 30 weeks.

Probably not a fit

Patients with major congenital defects or unstable conditions as determined by their neonatologist may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to identify early biomarkers associated with bronchopulmonary dysplasia (BPD) in infants born at less than 30 weeks gestational age. Researchers will collect various samples, including breath, throat swabs, and placental samples, to analyze volatile organic compounds, airway mucins, and the microbiome. The study will monitor infants for the development of BPD, diagnosed at 36 weeks postmenstrual age based on respiratory support needs. Follow-up visits at 6 and 12 months will assess lung function and microbiome composition.

Why it matters

Potential benefit: If successful, this study could lead to earlier identification and targeted interventions for infants at risk of developing BPD, potentially improving outcomes.

How similar studies have gone: While the approach of using biomarkers for early prediction of BPD is promising, it remains largely novel and untested in this specific context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Born at a gestational age \< 30 weeks

Exclusion Criteria:

* Major congenital defect or disorder
* Patients with an unstable general condition as deemed by the attending neonatologist

Where it's running

  • University Hospital Antwerp
    Edegem, Antwerp, Belgium
    Recruiting

Study contacts

  • Principal investigator: Antonius Mulder, MD, PhD,prof — University Hospital Antwerp, Belgium
  • Study coordinator: Inès Ghys, MD
  • Email: ines.ghys@uantwerpen.be
  • Phone: +3232655230

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.