CompletedNCT03808402
The Effect of Surfactant Dose on Outcomes in Preterm Infants With RDS
Studying Bronchopulmonary dysplasia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Chiesi UK
- Principal Investigator
- Kevin Goss, MBBS, M.DLeeds Teaching Hospitals NHS Trust
- Enrollment
- 2973 enrolled
- Eligibility
- All sexes
- Timeline
- 2018 – 2024
Study locations (29)
- William Harvey Hospital, Ashford, Kent, United Kingdom
- Birmingham Women's Hospital, Birmingham, United Kingdom
- Birmigham Heartlands Hospital, Birmingham, United Kingdom
- Royal Bolton Hospital, Bolton, United Kingdom
- Bradford Royal Infirmary, Bradford, United Kingdom
- Burnley General Hospital, Burnley, United Kingdom
- The Rosie Hospital, Cambridge, United Kingdom
- St Peter's Hospital, Chertsey, United Kingdom
- University Hospital Coventry, Coventry, United Kingdom
- Hull Royal Infirmary, Hull, United Kingdom
- Leeds General Infirmary, Leeds, United Kingdom
- Leicester Royal Infirmary, Leicester, United Kingdom
- Liverpool Women's Hospital, Liverpool, United Kingdom
- Homerton Hospital, London, United Kingdom
- University College Hospital, London, United Kingdom
- +14 more locations on ClinicalTrials.gov
Collaborators
The Leeds Teaching Hospitals NHS Trust · Imperial College London
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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