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Clinical Trials/NL-OMON48518
NL-OMON48518CompletedNot Applicable

mbilical oximetry during the neonatal transition: a feasibility study - PULSE study (Placing UmbiLical Sensor Early at birth study)

eids Universitair Medisch Centrum0 sites21 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
21

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
2 to 11 (—)

Inclusion Criteria

  • Healthy infants born at Leiden University Medical Centre birth centre.
  • Gestational age of at least 37 weeks, of multiparous mothers
  • No need for resuscitation/respiratory support

Exclusion Criteria

  • significant congenital malformations influencing the cardiopulmonary transition
  • signs of placental abruption or placenta praevia
  • signs of severe fetal distress necessitating an emergency caesarean section
  • infants needing respiratory support during transition as the cord will then be
  • clamped immediately
  • infants born via caesarean section
  • infants with short umbilical cords, that are unable to be placed at their
  • mothers chest

Investigators

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