Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT03094039

Initiation of Resuscitation While Attached to the Cord With Congenital Diaphragmatic Hernia

Initiation of Resuscitative Care While on Placental Circulation for Infants With Congenital Diaphragmatic Hernia - a Randomized Pilot Trial

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of Alberta · Academic / Other
Sex
All
Age
10 Minutes
Healthy volunteers
Not accepted

Summary

This study aims to measure the cardio-respiratory physiological consequences of initiating resuscitation during placental transfusion (PT) with an intact umbilical cord in infants with congenital diaphragmatic hernia (CDH). PT, mainly via delayed cord clamping, has been shown to offer a higher circulating blood volume, less need for blood transfusion, less need for inotropes in infants. Currently infants with CDH receive immediate cord clamping (ICC) to facilitate immediate resuscitation including immediate intubation and mechanical ventilation. With the development of a resuscitation platform (iNSPiRE), resuscitative care can now be commenced from birth in infants with CDH to benefit from PT.

Conditions

Interventions

TypeNameDescription
PROCEDUREVentilatory support while attached to the cordInfants will receive active resuscitative care (intubation and ventilation) using a specific designed platform for 120 seconds during delayed cord clamping. Then the cord will be clamped forgoing resuscitation care.
PROCEDUREImmediate cord clampingInfants will receive immediate cord clamping, transferred to the resuscitation table, intubated and mechanical ventilated according to our current Congenital Diaphragm Hernia protocol.

Timeline

Start date
2017-04-27
Primary completion
2019-08-31
Completion
2019-08-31
First posted
2017-03-29
Last updated
2019-10-03

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03094039. Inclusion in this directory is not an endorsement.