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Umbilical Cord Milking Versus Immediate Cord Clamping in Full Term Neonates (≥ 37 Weeks) Requiring Resuscitation

Not Applicable
Completed
Conditions
Perinatal Asphyxia
Hypoxic-Ischemic Encephalopathy
Interventions
Procedure: Umbilical cord milking
Procedure: Immediate cord clamping
Registration Number
NCT06090968
Lead Sponsor
Lady Hardinge Medical College
Brief Summary

The objective of the study is to compare the incidence of Hypoxic ischemic encephalopathy (all stages) among singleton term neonates (≥ 37 weeks) requiring resuscitation who will undergo Umbilical cord milking as compared to Immediate cord clamping.

Detailed Description

Enrolled participants will be randomly allocated to one of two study groups: 1) Umbilical cord clamping, 2) Immediate cord clamping

Umbilical cord clamping group: In the babies requiring resuscitation during vaginal delivery, the delivering obstetrician will place the infant on the mother's abdomen and about 20 cm of umbilical cord would be milked towards the infant with intact umbilical cord. The cord milking will be done four times by the obstetrical provider or by a second team member at the rate of 20 cm/2 sec. This procedure can be done in 15-20 seconds. Length of 20 cm can be estimated by the length of a sponge holding forceps which is approximately 25 cm. The umbilical cord will then clamped 2 -3 cm from the umbilical stump.

Immediate cord clamping: This will occur by clamping the umbilical cord as soon as possible (average 30 seconds).

Further resuscitation will be done in accordance with NRP 2015 guidelines. Stop watch will be used to calculate the duration after which the cord is clamped and cut, time to first breath, and time required to achieve HR \> 100/min

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
200
Inclusion Criteria

Vaginally born, Singleton Term gestation (≥ 37 and & < 42 weeks), requiring resuscitation at birth

Exclusion Criteria
  • Major congenital anomaly (antenatally diagnosed or visible at birth)
  • Rh negative pregnancy
  • Hydrops
  • Abruptio Placneta/ Placenta previa
  • Fetus with absent and reversal of End Diastolic flow
  • Cord avulsion
  • Refusal of consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Umbilical cord milkingUmbilical cord milking20 cm of umbilical cord would be milked towards the infant with intact umbilical cord. The cord milking will be done four times. The entire procedure can be done in 15-20 seconds
Immediate cord clampingImmediate cord clampingclamping the umbilical cord as soon as possible (average 30 seconds)
Primary Outcome Measures
NameTimeMethod
Incidence of Hypoxic Ischemic EncephalopathyFrom date of birth until date of death from any cause whichever come first assessed till 1 week of life

any stage as per Sarnat and Sarnat Staging

Secondary Outcome Measures
NameTimeMethod
Proportion requiring NICU admissionTill 1 week of life

NICU admission due to any reason

Neonates requiring Initial steps of resuscitation, Bag and Mask Ventilation, Intubation, chest compression and administration of drugs during resuscitation.Till 1 minutes of life

As per NRP 2015 guidelines

Proportion of neonates developing polycythemiaTill first 72 hours

Polycythemia is defined as venous hematocrit \>65%

Proportion of mortality due to any causeFrom date of birth until date of death from any cause whichever come first assessed till 4 week of life

Including early and late neonatal deaths

Hyperbilirubinemia requiring phototherapyFrom date of birth until date of death from any cause whichever come first assessed till 4 week of life

As per AAP charts

Level of hypoxic ischemic encephalopathy ( mild, moderate or severe)From date of birth until date of death from any cause whichever come first assessed till 1 week of life

Level of hypoxic ischemic encephalopathy as per Sarnat and Sarnat Staging

Mean Blood Pressure at 2,6,12,24,48,72 hrsFrom date of birth until date of death from any cause whichever come first assessed till 72 hours of life

Mean Blood Pressure as assessed by non-invasive oscillometric method

Received blood products or saline bolus or inotropes to support blood pressureFrom date of birth until date of death from any cause whichever come first assessed till 1 week of life

Hypotension requiring blood products or saline bolus or inotropes

Length of hospital stayFrom date of birth until date of death from any cause whichever come first assessed till 4 week of life

Duration of stay in days

Proportion of neonates having APGAR score < 4 at 5 minutes of lifeTill 5 minutes of life

APGAR score (Min zero maximum Ten) assessed at 1,5 minutes (Low APGAR is bad prognosis and High APGAR is good prognosis)

Trial Locations

Locations (1)

Lady Hardinge Medical college

🇮🇳

New Delhi, Delhi, India

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