Status:

COMPLETED

The Effect of Surfactant Dose on Outcomes in Preterm Infants With RDS

Lead Sponsor:

Chiesi UK

Collaborating Sponsors:

The Leeds Teaching Hospitals NHS Trust

Imperial College London

Conditions:

Respiratory Distress Syndrome

Bronchopulmonary Dysplasia

Eligibility:

All Genders

Brief Summary

A prospective observational study using de-identified data from the Neonatal Network Research Database (NNRD) supplemented by additional information on dose, method of surfactant administration and do...

Detailed Description

The rationale for this study is the clinical relevance of understanding whether surfactant dose affects neonatal outcomes in infants with RDS who are treated in the immediate postnatal period. In a r...

Eligibility Criteria

Inclusion

  • \<37 weeks gestational age Requiring surfactant for Respiratory Distress Syndrome Record of birth weight available Born after study initiation

Exclusion

  • 37 weeks gestation age or above Parental opt-out

Key Trial Info

Start Date :

October 26 2018

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 30 2024

Estimated Enrollment :

2973 Patients enrolled

Trial Details

Trial ID

NCT03808402

Start Date

October 26 2018

End Date

March 30 2024

Last Update

May 31 2025

Active Locations (29)

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Page 1 of 8 (29 locations)

1

William Harvey Hospital

Ashford, Kent, United Kingdom, TN24 0LZ

2

Birmingham Women's Hospital

Birmingham, United Kingdom, B15 2TG

3

Birmigham Heartlands Hospital

Birmingham, United Kingdom, B9 5SS

4

Royal Bolton Hospital

Bolton, United Kingdom, BL4 0JR

The Effect of Surfactant Dose on Outcomes in Preterm Infants With RDS | DecenTrialz