Autologous Umbilical Cord Blood Transfusion for Preterm Neonates

Status Withdrawn

Clinical Trial Summary

This is a pilot study to test feasibility of collection, preparation and infusion of a baby's own (autologous) umbilical cord blood in the first 14 days after birth if the baby is born premature <35 weeks of gestation.

Clinical Trial Description

In Egypt, 12-15.8% of live neonates are low birth weight and it is estimated that about one third of such infants are preterm [1] (UNICEF, 2001). In a study that Campbell et al. (2004) conducted in Egypt, the neonatal mortality rate was estimated to be 25 per 1000 live births. prematurity was considered the main cause of neonatal deaths (39%), followed by asphyxia (18%), infection (7%), especially in the late neonatal period, and congenital malformations (6%). A substantial proportion (29%) could not be classified [2]. In developing countries, prematurity was the main cause of early neonatal deaths (62%)[3] Autologous cord blood transfusion will be safe, and cheap. The preterm neonates need transfusion of whole blood or any of its components at a time during NICU admission. ;

Study Design

Related Conditions & MeSH terms

Anemia of Prematurity
Cerebral Hemorrhage
Hemorrhage
Intraventricular Hemorrhage
Premature Birth
Prematurity
Respiratory Distress Syndrome
Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Newborn

Clinical Trial Details

NCT number	NCT01121328
Study type	Interventional
Source	Ain Shams University
Contact
Status	Withdrawn
Phase	Phase 1
Start date	July 2011
Completion date	September 2014

View Details

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