The Study on Umbilical Cord Milking to Prevent and Decrease the Severity of Anemia in Preterms
Primary Purpose
Anemia
Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
umbilical cord milking
umbilical cord clamping immediately
Sponsored by
About this trial
This is an interventional prevention trial for Anemia focused on measuring umbilical cord milking;anemia;placental transfusion
Eligibility Criteria
Inclusion Criteria:
- Women in labour or with a plan for delivery at a gestational age less than 34 weeks gestation.
- Singleton pregnancy
- informed consent was obtained from the parent
Exclusion Criteria:
- Multiple gestation
- Diagnosis of any of the following in the current pregnancy: hemorrhage requiring clinic/hospital admission, placental abnormalities, fetal anomalies, Down's syndrome of the fetus,anemia
- Diagnosis of pre-eclampsia or eclampsia in current or previous pregnancies
- Diagnosis at any time for the mother of any of the following: serious Diabetes, serious hypertension, chronic renal disease
- Infant with major congenital malformation
- Infant with blood disease
- Unwilling to return for follow-up study visits at the hospital
Sites / Locations
- Xinhua Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
umbilical cord clamping immediately
umbilical cord milking
Arm Description
Umbilical cord was clamped immediately, or as close as possible, after delivery of the infant's shoulders. (This was standard practice in the study hospital, thus it served as the "control" group).
preterm baby were placed at or below level of the placenta and about 25cm of the umbilical cord was vigorously milked towards the umbilicus two to three times before clamping the cord. The milking speed was about 25cm/2 seconds
Outcomes
Primary Outcome Measures
concentrations of Hemoglobin (Hb)
concentrations of Hematocrit(Hct)
serum ferritin level
Secondary Outcome Measures
Hyperbilirubinemia requiring phototherapy
Hyperbilirubinemia requiring phototherapy (as per routine unit practice)
incidence and numbers of blood transfusions
Length of admission
complication
composite of bronchopulmonary dysplasia , Necrotizing Enterocolitis , grade 3 or 4 intraventricular hemorrhage or periventricular leukomalacia , or death prior to discharge home
Full Information
NCT ID
NCT03023917
First Posted
January 3, 2017
Last Updated
October 24, 2020
Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Collaborators
Shanghai First Maternity and Infant Hospital, Yangpu District Central Hospital Affiliated to Tongji University
1. Study Identification
Unique Protocol Identification Number
NCT03023917
Brief Title
The Study on Umbilical Cord Milking to Prevent and Decrease the Severity of Anemia in Preterms
Official Title
The Study on Umbilical Cord Milking to Prevent and Decrease the Severity of Anemia in preterms--a Multi-center Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
June 30, 2017 (Actual)
Primary Completion Date
August 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Collaborators
Shanghai First Maternity and Infant Hospital, Yangpu District Central Hospital Affiliated to Tongji 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 overall objective of the present study is to examine the effects of umbilical cord milking at birth in preterm infants to prevent and decrease anemia using a multi-center prospective randomized controlled trial comparing immediate cord clamping (standard at present) with umbilical cord milking.
Detailed Description
Anemia is a significant problem for pre-term infants and a major risk factor for preterm babies mortality and morbidity in neonatal intensive care unit(NICU). the majority of pre-term babies will require one or more blood transfusions during in NICU. Blood transfusion is a safe procedure but like all therapeutic interventions has risks associated with it and effort is made to reduce the number of transfusions that infants require during their stay on the neonatal unit.
Delayed cord clamping has a beneficial effect on prevention of anemia in later infancy because of increased iron stores at birth. However there are controversies in incorporating delayed cord clamping practice in the management of third stage of labour globally. Concerning about the need for urgent resuscitation and temperature management, attendants encouraged to clamp the umbilical cord immediately so that post-natal resuscitation and care can start as soon as possible.However,umbilical cord milking allows for swift intervention and resuscitation and attention to thermal care and should take less than 10 seconds to complete.
The specific aim of this study is to investigate the effects of umbilical cord milking on preventing and decreasing anemia in very pre-term infants.
Primary Outcomes:
Hemoglobin (Hb), Hematocrit (Hct) and serum iron levels at birth, at 1 week,at 2 weeks of age.
Secondary Outcomes:
Hemoglobin,hematocrit levels at 6 months of age.
Anemia at 1 week of life and 6 months follow-up, defined as hemoglobin levels below the respective cutoffs.
number of blood transfusions until 3 months corrected gestational age (CGA).
short term clinical profile of neonates like jaundice, polycythemia etc.
preterm infant complications such as lung function as assessed by oxygen dependency at 36 weeks corrected gestational age (CGA), and cardiovascular function as assessed by the need for volume expansion, inotropes, or clinically suspected patent ductus arteriosus(PDA )requiring intervention prior to discharge home,incidence of intraventricular hemorrhage and late-onset sepsis,etc.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia
Keywords
umbilical cord milking;anemia;placental transfusion
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
284 (Actual)
8. Arms, Groups, and Interventions
Arm Title
umbilical cord clamping immediately
Arm Type
Active Comparator
Arm Description
Umbilical cord was clamped immediately, or as close as possible, after delivery of the infant's shoulders. (This was standard practice in the study hospital, thus it served as the "control" group).
Arm Title
umbilical cord milking
Arm Type
Experimental
Arm Description
preterm baby were placed at or below level of the placenta and about 25cm of the umbilical cord was vigorously milked towards the umbilicus two to three times before clamping the cord. The milking speed was about 25cm/2 seconds
Intervention Type
Procedure
Intervention Name(s)
umbilical cord milking
Intervention Description
Infants were placed at or below level of the placenta and about 25cm of the umbilical cord was vigorously milked towards the umbilicus two to three times before clamping the cord. The milking speed was about 25cm/2 seconds
Intervention Type
Procedure
Intervention Name(s)
umbilical cord clamping immediately
Intervention Description
umbilical cord was cut immediately after birth
Primary Outcome Measure Information:
Title
concentrations of Hemoglobin (Hb)
Time Frame
48 hours after birth
Title
concentrations of Hematocrit(Hct)
Time Frame
48 hours after birth
Title
serum ferritin level
Time Frame
48 hours after birth
Secondary Outcome Measure Information:
Title
Hyperbilirubinemia requiring phototherapy
Description
Hyperbilirubinemia requiring phototherapy (as per routine unit practice)
Time Frame
during first 2 weeks of age
Title
incidence and numbers of blood transfusions
Time Frame
until 3 months corrected gestational age
Title
Length of admission
Time Frame
Birth to discharge, expected average of 30 days
Title
complication
Description
composite of bronchopulmonary dysplasia , Necrotizing Enterocolitis , grade 3 or 4 intraventricular hemorrhage or periventricular leukomalacia , or death prior to discharge home
Time Frame
Birth to discharge, expected average of 30 days
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women in labour or with a plan for delivery at a gestational age less than 34 weeks gestation.
Singleton pregnancy
informed consent was obtained from the parent
Exclusion Criteria:
Multiple gestation
Diagnosis of any of the following in the current pregnancy: hemorrhage requiring clinic/hospital admission, placental abnormalities, fetal anomalies, Down's syndrome of the fetus,anemia
Diagnosis of pre-eclampsia or eclampsia in current or previous pregnancies
Diagnosis at any time for the mother of any of the following: serious Diabetes, serious hypertension, chronic renal disease
Infant with major congenital malformation
Infant with blood disease
Unwilling to return for follow-up study visits at the hospital
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
guangyu chen
Organizational Affiliation
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
Xinhua Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200092
Country
China
12. IPD Sharing Statement
Plan to Share IPD
No
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The Study on Umbilical Cord Milking to Prevent and Decrease the Severity of Anemia in Preterms
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