Creating and maintaining functional residual capacity in preterm neonates with Respiratory Distress Syndrome (RDS)

Completed

• Conditions: Respiratory; Respiratory Distress Syndrome, Preterm neonates; Respiratory Distress Syndrome

• Registration Number: ISRCTN12757724
• Lead Sponsor: eiden University Medical Centre (LUMC) (Netherlands)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2005-12-20
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 200

Inclusion Criteria

1. Preterm neonates
2. Gestational age range 25 - 32 weeks (more than 24 weeks and 6 days and not more than 32 weeks and 6 days)

Exclusion Criteria

Antenatal diagnosed congenital anomalies of the cardio or respiratory system or anomalies incompatible with survival.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
eed of endotracheal intubation within 3 days after birth.

Secondary Outcome Measures

Name	Time	Method
1. Death<br>2. Bronchopulmonary Dysplasia (BPD)