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

Primary Purpose

Cardiac Output, High, Cardiac Output, Low

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Delayed cord clamping
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Cardiac Output, High

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Cairo University Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

30 second cord clamping

120 second cord clamping

Arm Description

Infants in this group will receive delayed cord clamping for 30 seconds.

Infants in this group will receive delayed cord clamping for 120 seconds.

Outcomes

Primary Outcome Measures

Cardiac output
Data imported from the electrical cardiometry device
Stroke volume
Data imported from the electrical cardiometry device
Cardiac index
Data imported from the electrical cardiometry device
Index of contractility
Data imported from the electrical cardiometry device
Heart rate
Data imported from the electrical cardiometry device
Oxygen saturation
Data imported from the electrical cardiometry device

Secondary Outcome Measures

Hemoglobin concentration
Blood sample will be obtained an analyzed
Serum glucose concentration
Blood sample will be obtained an analyzed
Serum bilirubin concentration
Blood sample will be obtained an analyzed

Full Information

First Posted
April 18, 2020
Last Updated
April 21, 2020
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT04358822
Brief Title
Hemodynamic Effects of Delayed Umbilical Cord Clamping in Full-term Newborns
Official Title
Hemodynamic Effects of Delayed Umbilical Cord Clamping in Full-term Newborns
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
January 21, 2020 (Actual)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
March 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed 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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Output, High, Cardiac Output, Low

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
68 (Actual)

8. Arms, Groups, and Interventions

Arm Title
30 second cord clamping
Arm Type
Active Comparator
Arm Description
Infants in this group will receive delayed cord clamping for 30 seconds.
Arm Title
120 second cord clamping
Arm Type
Active Comparator
Arm Description
Infants in this group will receive delayed cord clamping for 120 seconds.
Intervention Type
Procedure
Intervention Name(s)
Delayed cord clamping
Intervention Description
The umbilical cord will be clamped after specific time intervals
Primary Outcome Measure Information:
Title
Cardiac output
Description
Data imported from the electrical cardiometry device
Time Frame
at 15 minutes
Title
Stroke volume
Description
Data imported from the electrical cardiometry device
Time Frame
at 15 minutes
Title
Cardiac index
Description
Data imported from the electrical cardiometry device
Time Frame
at 15 minutes
Title
Index of contractility
Description
Data imported from the electrical cardiometry device
Time Frame
at 15 minutes
Title
Heart rate
Description
Data imported from the electrical cardiometry device
Time Frame
at 15 minutes
Title
Oxygen saturation
Description
Data imported from the electrical cardiometry device
Time Frame
at 15 minutes
Secondary Outcome Measure Information:
Title
Hemoglobin concentration
Description
Blood sample will be obtained an analyzed
Time Frame
At 24 hours
Title
Serum glucose concentration
Description
Blood sample will be obtained an analyzed
Time Frame
At 24 hours
Title
Serum bilirubin concentration
Description
Blood sample will be obtained an analyzed
Time Frame
At 24 hours

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reem Mahmoud
Organizational Affiliation
Cairo University Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cairo University Children's Hospital
City
Cairo
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27057332
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.
Results Reference
background
PubMed Identifier
30021580
Citation
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.
Results Reference
background
PubMed Identifier
26890553
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.
Results Reference
background
PubMed Identifier
27929530
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.
Results Reference
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Hemodynamic Effects of Delayed Umbilical Cord Clamping in Full-term Newborns

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