Comparative Outcomes Related to Delivery-room Cord Milking In Low-resourced Kountries Developmental Follow Up

Recruiting N/A Interventional Study
Hypoxic-Ischemic Encephalopathy Birth Asphyxia
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
22 Months – 26 Months
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
3,442 (estimated)
Sponsor
Nemours Children's Clinic · Other
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About This Trial

An extension of the CORDMILK trial, the CORDMILK follow-up trial will evaluate the neurodevelopmental outcomes at 22-26 months age of term/late preterm infants who were non-vigorous at birth and received umbilical cord milking (UCM) or early cord clamping (ECC).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Enrolled in CORDMILK trial * Non-vigorous at birth Exclusion Criteria: * None
Contacts

Zubair H Aghai, MD

215 955 6523

zaghai@nemours.org

CONTACT

Anup Katheria, MD

858 839 4170

anup.katheria@sharp.com

CONTACT