The Effect of Time Window for Umbilical Cord Clamping During Cesareans on Offspring Hemoglobin and Maternal Blood Loss
Primary Purpose
Delayed Cord Clamping, Hemoglobin, Blood Loss
Status
Active
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Delayed cord clamping (30s)
Delayed cord clamping (60s)
Delayed cord clamping (90s)
Sponsored by
About this trial
This is an interventional prevention trial for Delayed Cord Clamping focused on measuring Cesarean delivery, Time window for umbilical cord clamping, Maternal and neonatal health outcome, Anemia, Randomized controlled trial
Eligibility Criteria
Inclusion Criteria:
- local resident in Liuyang city, Huantai county and their surrounding areas
- Singleton pregnancy
- Elective caesarean, or cesarean section after the start of labor but the cervix is less than 3 cm
- Term pregnancy (≥37 weeks of gestation), and the fetal weight was estimated ≥2500g by intrauterine ultrasound
- Written informed consent is obtained
Exclusion Criteria:
- Pregnant women with the following risk factors: severe hypertension (systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥110mmHg), preeclampsia, chronic hypertension with preeclampsia, diabetes mellitus with severe microangiopathy, placenta previa, placenta implantation, placental abruption, intrauterine distress, prenatal infection, severe anemia (hemoglobin<7g/dL), coagulation disorders, thrombosis disease
- Plan to retain cord blood
- Rh-negative pregnant women
- Prenatal diagnosis of fetal abnormalities which may lead to difficulties in cesareans or adverse pregnancy outcomes, such as abnormal heart monitoring, fetal distress, malformation, anemia, and intrauterine growth restrictions
- Other conditions not suitable for intervention as judged by obstetricians
Sites / Locations
- Liuyang Maternal and Child Health Care Hospital
- Women and Children's Health Care Hospital of Huantai
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
No Intervention
Arm Label
Delay 30s group
Delay 60s group
Delay 90s group
Control group
Arm Description
Cord clamping will be delayed at 30 seconds after delivery.
Cord clamping will be delayed at 60 seconds after delivery.
Cord clamping will be delayed at 90 seconds after delivery.
Cord clamping will be immediate (within 15 seconds) after delivery, in accordance with the standard practice in the study sites
Outcomes
Primary Outcome Measures
The neonatal hemoglobin
In the heel blood
The change in maternal hemoglobin
Difference in maternal hemoglobin levels before and after the cesarean
Secondary Outcome Measures
The incidence rate of neonatal anemia
Defined as hemoglobin <145g/L
The incidence rate of neonatal jaundice
The incidence rate of neonatal jaundice
Apgar score
An indicator for the activity, pulse, grimace, appearance, and respiration of neonates. It ranges from 0 to 10, the higher the better.
The incidence rate of neonatal intensive care unit admission
The incidence rate of neonatal intensive care unit admission
Placental weight
In grams
Maternal hemoglobin after the cesarean
In venous blood
Estimated maternal blood loss
By volume-method and area-method
The incidence rate of maternal blood transfusion
The incidence rate of maternal blood transfusion
Full Information
NCT ID
NCT05492214
First Posted
August 2, 2022
Last Updated
May 30, 2023
Sponsor
Peking University
Collaborators
National Natural Science Foundation of China, Liuyang Maternal and Child Health Care Hospital, Women and Children's Health Care Hospital of Huantai
1. Study Identification
Unique Protocol Identification Number
NCT05492214
Brief Title
The Effect of Time Window for Umbilical Cord Clamping During Cesareans on Offspring Hemoglobin and Maternal Blood Loss
Official Title
The Effect of Time Window for Umbilical Cord Clamping During Cesarean Section on the Health Outcomes of Offspring Hemoglobin and Maternal Blood Loss
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 22, 2022 (Actual)
Primary Completion Date
May 8, 2023 (Actual)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking University
Collaborators
National Natural Science Foundation of China, Liuyang Maternal and Child Health Care Hospital, Women and Children's Health Care Hospital of Huantai
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
This is a randomized controlled trial, aiming to evaluate the effects of time window for umbilical cord clamping during cesarean section on the health outcomes of offspring hemoglobin,maternal blood loss,and children's growth and development. It will be conducted in Liuyang city and Huantai county of China, and the targeted sample size is 360 (180 in each site). All the eligible pregnant women will be randomly assigned to one of the four groups (three intervention groups and one control group), and their babies will be followed up to 18 months of age.
Detailed Description
The World Health Organization and American College of Obstetricians and Gynecologists have recommended a delay in umbilical cord clamping after birth, irrespective of delivery modes, which was based on studies from vaginal deliveries rather than cesareans. In cesareans, the optimal time window for umbilical cord clamping has not been determined, and the relevant safety data are limited. In this randomized study, the investigators aim to evaluate the impacts of time window for umbilical cord clamping during cesarean section on maternal and child health outcomes, and to evaluate the optimal timing of the clamping. The investigators are planning to enroll 360 pregnant women scheduled for cesareans, and to randomly allocate them into four groups: the umbilical cord will be clamped within 15 seconds (immediately), or delayed after deliveries for 30, 60, and 90 seconds, respectively. Babies will be followed up at 3, 6, 12, and 18 months of age. Maternal hemoglobin before and after cesareans, neonatal hemoglobin, children's hemoglobin at 6, 12, 18 months of age will be measured. At each follow-up visit, children's length and weight will be measured, their development will be assessed, and a questionnaire survey including information on feeding, sleep, and medication will be conducted. The primary outcomes are the neonatal hemoglobin and the change in maternal hemoglobin. The secondary outcomes include the incidence rate of neonatal anemia and jaundice, Apgar score, the incidence rate of neonatal intensive care unit (NICU) admission, placental weight, maternal hemoglobin after the cesarean, estimated maternal blood loss, and the incidence rate of maternal blood transfusion. In addition, the children's hemoglobin, anemia, growth and development are considered as the exploratory secondary outcomes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delayed Cord Clamping, Hemoglobin, Blood Loss
Keywords
Cesarean delivery, Time window for umbilical cord clamping, Maternal and neonatal health outcome, Anemia, Randomized controlled trial
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
360 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Delay 30s group
Arm Type
Experimental
Arm Description
Cord clamping will be delayed at 30 seconds after delivery.
Arm Title
Delay 60s group
Arm Type
Experimental
Arm Description
Cord clamping will be delayed at 60 seconds after delivery.
Arm Title
Delay 90s group
Arm Type
Experimental
Arm Description
Cord clamping will be delayed at 90 seconds after delivery.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Cord clamping will be immediate (within 15 seconds) after delivery, in accordance with the standard practice in the study sites
Intervention Type
Procedure
Intervention Name(s)
Delayed cord clamping (30s)
Intervention Description
The same as that stated in arm descriptions.
Intervention Type
Procedure
Intervention Name(s)
Delayed cord clamping (60s)
Intervention Description
The same as that stated in arm descriptions.
Intervention Type
Procedure
Intervention Name(s)
Delayed cord clamping (90s)
Intervention Description
The same as that stated in arm descriptions.
Primary Outcome Measure Information:
Title
The neonatal hemoglobin
Description
In the heel blood
Time Frame
Within 72 hours after birth
Title
The change in maternal hemoglobin
Description
Difference in maternal hemoglobin levels before and after the cesarean
Time Frame
Within 72 hours before the cesarean, and within 72 hours after the cesarean
Secondary Outcome Measure Information:
Title
The incidence rate of neonatal anemia
Description
Defined as hemoglobin <145g/L
Time Frame
Within 72 hours after birth
Title
The incidence rate of neonatal jaundice
Description
The incidence rate of neonatal jaundice
Time Frame
Before discharging from hospitals, usually within 1 week after birth
Title
Apgar score
Description
An indicator for the activity, pulse, grimace, appearance, and respiration of neonates. It ranges from 0 to 10, the higher the better.
Time Frame
At 1 min, 5 min, and 10 min after birth
Title
The incidence rate of neonatal intensive care unit admission
Description
The incidence rate of neonatal intensive care unit admission
Time Frame
Before discharging from hospitals, usually within 1 week after birth
Title
Placental weight
Description
In grams
Time Frame
At birth
Title
Maternal hemoglobin after the cesarean
Description
In venous blood
Time Frame
Within 72 hours after the cesarean
Title
Estimated maternal blood loss
Description
By volume-method and area-method
Time Frame
During the cesarean
Title
The incidence rate of maternal blood transfusion
Description
The incidence rate of maternal blood transfusion
Time Frame
At delivery
Other Pre-specified Outcome Measures:
Title
The children's hemoglobin
Description
In fingertip blood
Time Frame
At 6, 12, 18 months of age
Title
The children's anemia
Description
Defined as hemoglobin <110 g/L
Time Frame
At 6, 12, 18 months of age
Title
The children's length
Description
In Z-score
Time Frame
At 3, 6, 12, 18 months of age
Title
The children's weight
Description
In Z-score
Time Frame
At 3, 6, 12, 18 months of age
Title
The results of Denver Developmental Screening Test
Description
The abnormal rate
Time Frame
At 3, 6, 12, 18 months of age
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
local resident in Liuyang city, Huantai county and their surrounding areas
Singleton pregnancy
Elective caesarean, or cesarean section after the start of labor but the cervix is less than 3 cm
Term pregnancy (≥37 weeks of gestation), and the fetal weight was estimated ≥2500g by intrauterine ultrasound
Written informed consent is obtained
Exclusion Criteria:
Pregnant women with the following risk factors: severe hypertension (systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥110mmHg), preeclampsia, chronic hypertension with preeclampsia, diabetes mellitus with severe microangiopathy, placenta previa, placenta implantation, placental abruption, intrauterine distress, prenatal infection, severe anemia (hemoglobin<7g/dL), coagulation disorders, thrombosis disease
Plan to retain cord blood
Rh-negative pregnant women
Prenatal diagnosis of fetal abnormalities which may lead to difficulties in cesareans or adverse pregnancy outcomes, such as abnormal heart monitoring, fetal distress, malformation, anemia, and intrauterine growth restrictions
Other conditions not suitable for intervention as judged by obstetricians
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jianmeng Liu
Organizational Affiliation
Peking University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hongtian Li
Organizational Affiliation
Peking University
Official's Role
Study Director
Facility Information:
Facility Name
Liuyang Maternal and Child Health Care Hospital
City
Liuyang
State/Province
Hunan
ZIP/Postal Code
410399
Country
China
Facility Name
Women and Children's Health Care Hospital of Huantai
City
Zibo
State/Province
Shandong
ZIP/Postal Code
256499
Country
China
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
The IPD will be shared upon the request of other researchers, and all the key variables that will be reported in the main paper are planned to be shared
IPD Sharing Time Frame
After the publication of the main paper (hopefully before the end of 2024), the data will be available to share to other researchers
IPD Sharing Access Criteria
Researchers should request the data via the following Email: lihongtian@pku.edu.cn or liujm@pku.edu.cn
Learn more about this trial
The Effect of Time Window for Umbilical Cord Clamping During Cesareans on Offspring Hemoglobin and Maternal Blood Loss
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