- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03657394
Comparative Outcomes Related to Delivery-room Cord Milking In Low-resourced Kountries (CORDMILK)
A Cluster Randomized Clinical Trial of Umbilical Cord Milking Versus Early Cord Clamping on Short and Long-term Outcomes in Neonates Who Are Non-Vigorous at Birth
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hypoxic-ischemic encephalopathy (HIE) is a brain injury caused by inadequate blood flow and oxygen delivery to the neonatal brain. Almost all infants with severe HIE and 30-50% infants with moderate HIE either die or develop significant developmental delay, cerebral palsy or other disabilities.The incidence of HIE is 1-3 per 1,000 term births in developed countries and 15-20 times higher in developing countries (Worldwide, 0.5 to 1 million infants develop HIE each year). Therapeutic hypothermia is the only proven therapy for infants with HIE. Even after receiving therapeutic hypothermia, one-half of all infants with moderate and severe HIE die or develop neurological and functional impairment. Therapeutic hypothermia is not widely available and ineffective in developing nations.There is an urgent need for a new therapy for neonates with HIE, which can complement hypothermia and be readily available in developing nations. Stem cell transplantation is a potential therapy for infants with HIE. Umbilical cord blood is a rich source of stem cells. Umbilical cord milking (UCM) may have similar effect as autologous umbilical cord blood cell transplantation.
Preliminary evidence suggests a placental transfusion in term infants may be a neuroprotective mechanism that can also facilitate cardiovascular transition for neonates depressed at birth and result in decreased mortality and improved neurodevelopmental outcomes. Infants with HIE, due to varied complications during the birth process, have poor perfusion due to fetal blood volume loss to the placenta. However, the most common method of providing placental blood, delayed cord clamping (DCC) cannot be performed since infants with HIE are non-vigorous and providers often need to perform resuscitation immediately after birth. The World Health Organization and the American College of Obstetrics and Gynecology (ACOG) also does not recommended DCC in neonates who are non-vigorous (limp, pale, and not breathing) at birth and require immediate resuscitation. Umbilical cord milking (UCM) or gently squeezing cord blood toward the baby, is an alternative to DCC, which can achieve significant placental transfusion without delaying resuscitation. Further, UCM can be completed as quickly as immediate cord clamping (ICC) and UCM requires minimal training and no additional staff.
The investigators hypothesized that UCM will reduce the number of infants developing moderate to severe HIE or death in neonates who are non-vigorous at birth compared to early cord clamping (ECC). This will be a cluster crossover randomized controlled trial. Each hospital will be randomly assigned to use either ECC or UCM for any infant who is non-vigorous at birth and needing resuscitation over a period of 6 months. Then the site will change to the other method for an additional 6 months.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Karnataka
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Belagavi, Karnataka, India, 590010
- KLE Academy of Higher Education and Research (Deemed-to-be-University) Jawaharlal Nehru Medical College
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MS
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Chandrapur, MS, India, 442401
- Government Medical College
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Nagpur, MS, India, 440002
- Daga Memorial Woman and Children Hospital
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Nagpur, MS, India, 440009
- Government Medical College and Hospital
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Nagpur, MS, India, 441108
- All India Institute of Medical Science
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Wardha, MS, India, 442102
- Mahatma Gandhi Institute of Medical Sciences/ Kasturba Hospital
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Maharashtra
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Nagpur, Maharashtra, India, 440018
- Indira Gandhi Government Medical College & Hospital
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Pune, Maharashtra, India, 411018
- Pimpri Chinchwad Municipal Corporation's Post-Graduate Institute, Yashwantrao Chavan Memorial Hospital
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Rajasthan
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Jaipur, Rajasthan, India, 302004
- Sawai Man Singh (SMS) Medical College
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Non-vigorous neonates born between 35-42 weeks
Exclusion Criteria:
- Congenital malformation of CNS.
- Chromosomal abnormalities.
- Major congenital malformations.
- Abruption/cutting through the placenta at delivery.
- Umbilical cord knots or inadequate cord length.
- Mono-chorionic twins or twins with no information on amnion/chorion.
- Multiple gestation >2 .
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Umbilical Cord Milking
The delivering practitioner will place the newborn below the level of the incision (at the edge of the table) at C/S and a second team member will milk the cord four times.
For vaginal delivery, the delivering obstetrician, midwife or perinatal provider will hold the infant against their body or place the infant on the mother's abdomen and the cord will be milked either four times by the obstetrical provider or by a second team member.
For the cord milking procedure, the obstetrical provider will milk 20-30 centimeters length of the umbilical cord over two seconds, repeating three additional times as described previously.
This time is not significantly different from the time for ECC.
|
At delivery, the umbilical cord is grasped, and blood is pushed toward the infant 4 times before the cord is clamped.
This procedure infuses a placental transfusion of blood into the infant and can be done in 1--15 seconds.
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No Intervention: Early Cord Clamping
Umbilical cord will be clamped immediately after birth (within 60 seconds)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Moderate to severe HIE or death
Time Frame: From date of birth until the date of discharge from the hospital or date of death from any cause, whichever come first, asessed up to 10 weeks.
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Number of infants with moderate to severe HIE or death
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From date of birth until the date of discharge from the hospital or date of death from any cause, whichever come first, asessed up to 10 weeks.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
MRI of the brain
Time Frame: 4 days to 2 weeks
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Number of infants with moderate to severe HIE who have abnormal brain MRI
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4 days to 2 weeks
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Anup Katheria, MD, Sharp Mary Birch Hospital for Women & Newborns
- Principal Investigator: Zubair H Aghai, MD, Nemours Children's Clinic
- Principal Investigator: Sangappa Dhaded, MD, KLE Academy of Higher Education and Research
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Infant, Newborn, Diseases
- Brain Ischemia
- Hematologic Diseases
- Signs and Symptoms, Respiratory
- Anemia
- Hypoxia, Brain
- Hypoxia
- Anemia, Neonatal
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Hemic and Lymphatic Diseases
- Hypoxia-Ischemia, Brain
- Asphyxia Neonatorum
- Fetofetal Transfusion
- Surgical Procedures, Operative
- Delivery, Obstetric
- Obstetric Surgical Procedures
- Umbilical Cord Clamping
Other Study ID Numbers
- CORDMILK
- R01HD102967 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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