Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to determine if delayed cord clamping above the perineum has an effect on neonatal hematocrit when compared to delayed cord clamping below the perineum in pre-term spontaneous vaginal deliveries.


Clinical Trial Description

This study will compare the difference in neonatal hematocrit with delayed cord clamping above vs. below the perineum, in infants who are born via pre-term spontaneous vaginal deliveries that are vigorous at delivery. Delayed cord clamping below the perineum is an accepted clinical practice in obstetrics and gynecology; however, delayed cord clamping above the perineum has not yet been studied in preterm infants. Delayed cord clamping above the perineum will provide the benefit of immediate skin-to-skin contact between the mother and her newborn. Patients will have delayed cord clamping performed for 60-75 seconds either below the maternal perineum or while the infant is placed on the mother's abdomen. At approximately 24 hours after delivery (at the time of infant heel stick for routine, state-mandated screening tests), a small additional amount of blood will be collected to evaluate newborn hematocrit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02659605
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact
Status Completed
Phase N/A
Start date January 2016
Completion date February 2017

See also
  Status Clinical Trial Phase
Active, not recruiting NCT05492214 - The Effect of Time Window for Umbilical Cord Clamping During Cesareans on Offspring Hemoglobin and Maternal Blood Loss N/A
Completed NCT03150641 - Delayed Cord Clamping at Term Cesarean N/A
Completed NCT03878602 - Umbilical Cord Clamping: What Are the Benefits N/A
Completed NCT03147846 - The Hematologic Impact of Umbilical Cord Milking Versus Deferred Cord Clamping in Premature Neonates. N/A
Recruiting NCT05507424 - Prone Positioning During Delayed Cord Clamping N/A