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UnknownNCT03852134

Milking of the Cut-Cord During Resuscitation of Preterm Infants (The MOCC Study)

Milking of the Cut-Cord During Resuscitation of Preterm Infants: A Randomized Controlled Trial (The MOCC Study)

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
98 (estimated)
Sponsor
IWK Health Centre · Academic / Other
Sex
All
Age
1 Minute
Healthy volunteers
Not accepted

Summary

In this feasibility study, the investigators will randomize preterm infants born at \<32 weeks gestation to either the standard practice of delayed cord clamping (DCC) for 30-60 seconds at birth or milking of the long-cut cord (MOCC) while providing resuscitation/stabilization to the infant. The main objectives of the trial are to assess the feasibility of the new approach (MOCC) and to compare the two groups regarding the hemoglobin levels on admission to NICU in addition to neonatal morbidity and mortality.

Conditions

Interventions

TypeNameDescription
PROCEDUREMOCC GroupAfter 30 seconds of DCC, the cord will be clamped and cut 5 cm from the introitus in vaginal delivery or abdominal incision in the case of cesarean section before passing the infant with the long umbilical cord segment to the pediatric provider who will milk the cord one time towards the baby during resuscitation.
PROCEDUREDCC GroupThe OB provider will hold the baby at or below the level of placenta, provide warmth, stimulate the baby to breathe and suction the mouth/nose if needed for the first 30 seconds. After these initial 30 seconds, if the baby is breathing then the obstetrician will continue DCC for a total of 60 seconds before clamping and cutting the cord close to the umbilicus and handing over the baby to the neonatal team for further stabilization as per standard NRP practice. If the baby is not breathing after the initial 30 seconds of DCC, then the OB provider will clamp and cut the cord close to the umbilicus and hand over the baby to the neonatal team to continue resuscitation of the baby as per the standard NRP guidelines.

Timeline

Start date
2019-02-07
Primary completion
2021-02-07
Completion
2023-07-31
First posted
2019-02-25
Last updated
2019-02-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03852134. Inclusion in this directory is not an endorsement.