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Clinical Trials/NL-OMON23993
NL-OMON23993
Completed
Not Applicable

A randomized controlled trial of respiratory function monitoring during stabilization of preterm infants at birth

eids Universitair Medisch Centrum, Leiden, The Netherlands0 sites320 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
prematuriteit- prematurityresuscitatie-resuscitation
Sponsor
eids Universitair Medisch Centrum, Leiden, The Netherlands
Enrollment
320
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

/A

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
eids Universitair Medisch Centrum, Leiden, The Netherlands

Eligibility Criteria

Inclusion Criteria

  • Infants born will be included in this study if they are between 24 and 27 completed weeks gestation receiving PPV for resuscitation at birth and do not have a known abnormality which might interfere with breathing.

Exclusion Criteria

  • Infants will be excluded from the final analysis if they are found to have a congenital abnormality or condition that might have an adverse effect on breathing or ventilation, including: congenital diaphragmatic hernia, tracheo\-oesophageal fistula or cyanotic heart disease.

Outcomes

Primary Outcomes

Not specified

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