Hemodynamic Effects of Delayed Umbilical Cord Clamping in Full-term Newborns

Cardiac Output, Low Clinical Trial

Official title:

Hemodynamic Effects of Delayed Umbilical Cord Clamping in Full-term Newborns

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04358822
• Other study ID #: MS-305-2019
• Status: Completed
• Phase: N/A
• Start date: January 21, 2020
• Est. completion date: March 31, 2020

Study information

• Verified date: April 2020
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The sequence of events at the time of delivery includes delivery of the infant, clamping of the umbilical cord, and lastly delivery of the placenta. There are some benefits for delayed cord clamping. This study aims to compare the effects of two different duration of delayed cord clamping.

Infants will be randomized into two groups based on the duration of delayed cord clamping: 30 seconds vs 120 seconds. Different hemodynamic effects will be measured in each group at different time intervals. The hypothesis of the study is that delayed cord clamping for 120 seconds is associated with better cardiac output and with other hemodynamic advantages.

Description:

The study will include full term infants delivered via cesarean section. Written informed consent for participation in the study will be obtained from parents prior to delivery. Newborns will be randomly assigned into two groups according to the duration of cord clamping: Group 1: the cord will be clamped at 30 seconds, and Group 2: the cord will be clamped at 120 seconds of life. Stopwatch will be started when infants buttocks (or head if breech) are delivered from the uterus. The time elapsed will be counted aloud by the investigator in 10-second intervals. During this time, the infant will be held in linen on the mothers legs. Care will be taken not to apply traction on the cord. Milking of the cord will not be allowed. Immediately after resuscitation, infants will be attached to the leads of the electrical cardiometry device. Device output will be imported at 5, 10, and 15 minutes after birth in both groups. A follow up measurement will be imported later at 24 hours of age. In addition, a peripheral blood sample will be obtained at 24 hours of age for assessment of hemoglobin, glucose and bilirubin concentrations. .

The calculated sample size is 31 newborns in each group. This number will be adequate to detect an effect size of 10% in the mean cardiac output between the two groups with 95% confidence and 80% power. The study plans to recruit 34 infants in each group (10% attrition rate).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 68
• Est. completion date: March 31, 2020
• Est. primary completion date: March 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Normal full term newborns =37 weeks gestational age

• Both genders are included

• Singleton

• Delivered by elective cesarean section due to previous cesarean section, cephalo-pelvic disproportion, or mal-presentation

• Successfully transitioned without need for respiratory or medication support

Exclusion Criteria:

• Neonates needing any active resuscitation

• In-utero fetal distress

• Suspected perinatal asphyxia

• Major congenital malformations

• Twin or multiple gestation

• Intrauterine growth restriction

• Placenta previa

• Mothers with cardiac disorders

Related Conditions & MeSH terms

• Cardiac Output, High
• Cardiac Output, Low

Intervention

Procedure:
• Delayed cord clamping
The umbilical cord will be clamped after specific time intervals

Locations

Country	Name	City	State
Egypt	Cairo University Children's Hospital	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (4)

Chopra A, Thakur A, Garg P, Kler N, Gujral K. Early versus delayed cord clamping in small for gestational age infants and iron stores at 3 months of age - a randomized controlled trial. BMC Pediatr. 2018 Jul 18;18(1):234. doi: 10.1186/s12887-018-1214-8. — View Citation

Hsu KH, Wu TW, Wang YC, Lim WH, Lee CC, Lien R. Hemodynamic reference for neonates of different age and weight: a pilot study with electrical cardiometry. J Perinatol. 2016 Jun;36(6):481-5. doi: 10.1038/jp.2016.2. Epub 2016 Feb 18. — View Citation

Katheria AC, Wozniak M, Harari D, Arnell K, Petruzzelli D, Finer NN. Measuring cardiac changes using electrical impedance during delayed cord clamping: a feasibility trial. Matern Health Neonatol Perinatol. 2015 May 22;1:15. doi: 10.1186/s40748-015-0016-3. eCollection 2015. — View Citation

Mercer JS, Erickson-Owens DA, Collins J, Barcelos MO, Parker AB, Padbury JF. Effects of delayed cord clamping on residual placental blood volume, hemoglobin and bilirubin levels in term infants: a randomized controlled trial. J Perinatol. 2017 Mar;37(3):260-264. doi: 10.1038/jp.2016.222. Epub 2016 Dec 8. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cardiac output	Data imported from the electrical cardiometry device	at 15 minutes
Primary	Stroke volume	Data imported from the electrical cardiometry device	at 15 minutes
Primary	Cardiac index	Data imported from the electrical cardiometry device	at 15 minutes
Primary	Index of contractility	Data imported from the electrical cardiometry device	at 15 minutes
Primary	Heart rate	Data imported from the electrical cardiometry device	at 15 minutes
Primary	Oxygen saturation	Data imported from the electrical cardiometry device	at 15 minutes
Secondary	Hemoglobin concentration	Blood sample will be obtained an analyzed	At 24 hours
Secondary	Serum glucose concentration	Blood sample will be obtained an analyzed	At 24 hours
Secondary	Serum bilirubin concentration	Blood sample will be obtained an analyzed	At 24 hours