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Ventilation, inflammation, perfusion and structure in pediatric Bronchopulmonary dysplasia Erasmus

Ventilation, inflammation, perfusion and structure in pediatric Bronchopulmonary dysplasia Erasmus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21082
Enrollment
10
Registered
2018-06-08
Start date
2018-09-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchopulmonary dysplasia

Interventions

Spirometry, multiple breath washout and MRI

Sponsors

Erasmus MC- Sophia Children's Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosis of BPD according to the NHI criteria, aged between 6-10 years, will have/has a CT scan planned within 6 months of this research, informed consent by parents (and patient).

Exclusion criteria

Exclusion criteria: Inability to undergo MRI, inability to follow instructions in the MRI, current severe lung infection (symptoms of respiratory distress, severe coughing, antibiotic use), chronic oxygen use

Design outcomes

Primary

MeasureTime frame
The primary outcomes of this study are the pulmonary MR findings. All scans will be evaluated on changes in ventilation, inflammation, perfusion and structure. All data will be compared to the spirometry, LCI and MRI of two control groups: 1) premature non-BPD patients (born before <32 weeks without the diagnosis of BPD) 2) healthy volunteers.

Secondary

MeasureTime frame
A qualitative and feasibility check of all MRIs will be done. Furthermore, all the MRI findings will be compared to the spirometry and multiple breath washout measurements and a clinically ordered pulmonary CT made within six months of the research MRI.

Contacts

Public ContactH.A.W.M. Tiddens

Erasmus Medical Center, Sophia Children’s Hospital Rotterdam, Department of Pediatric Pulmonology, Dr. Molewaterplein 60

h.tiddens@erasmusmc.nl+31 (0)10 4636690 / +31 (0)10 4636363 (general)

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)