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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05951348
Other study ID # 0106748
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 11, 2021
Est. completion date June 20, 2022

Study information

Verified date May 2023
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the study is conducted on the different actions on umbilical cord clamping including immediate cord clamping (ICC) , delayed cord clamping (DCC) for 30 seconds and umbilical cord milking (UCM) for 10-15 seconds in females that are delivered by elective cesarean section , to assess the neonatal outcomes including Hemoglobin and Hematocrit levels after birth in the newborn and the bilirubin level after 72 hrs


Description:

the benefit of umbilical cord milking for 10-15 seconds maneuver in cesarean section, that short time can improve the hemoglobin level and prevent anemia in the newborn with improvement of the iron stores for months in infancy without affection on the bilirubin level and the need for phototherapy. This is significant because of the rising rate of cesarean section all over the world make more children are liable for anemia, and by this simple technique it can be prevented.


Recruitment information / eligibility

Status Completed
Enrollment 162
Est. completion date June 20, 2022
Est. primary completion date June 20, 2022
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - mother's age (20-40) years. - pregnancy with a healthy singleton - gestational age of 38-41 0/7 weeks - uncomplicated pregnancy Exclusion Criteria - Any medical or obstetrical complications like hypertension, pre-eclampsia, diabetes any special habits like smoking, and substance abuse - Rh-negative mothers. The fetal exclusion criteria - fetus with evidence of intrauterine growth restriction - infant with serious congenital anomalies.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Delayed cord clamping for 30 seconds
waiting for 30 seconds after delivery of the fetus or milking of the cord in the direction of the fetus 10 times in time frame 10-15 seconds

Locations

Country Name City State
Egypt Tamer Ahmed Hosny Alexandria

Sponsors (1)

Lead Sponsor Collaborator
Alexandria University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary hemoglobin level a blood sample is taken from the umbilical cord of the neonate immediately after the intervention
Secondary bilirubin level trans-cutaneous measurement of the bilirubin level 72 hours after delivery
See also
  Status Clinical Trial Phase
Completed NCT05551390 - Effect of One-time Versus Three-times of Umbilical Cord Milking on Neonatal Hemoglobin in Late Preterm N/A
Completed NCT03147846 - The Hematologic Impact of Umbilical Cord Milking Versus Deferred Cord Clamping in Premature Neonates. N/A
Completed NCT02287077 - Umbilical Cord Milking for Neonates With Hypoxic Ischemic Encephalopathy N/A
Active, not recruiting NCT03200301 - Effect of Intact Umbilical Cord Milking on Neonatal and First Year Neurodevelopmental Outcomes in Very Preterm Infants. N/A