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Determination of Heart Rate in Infants Needing Resuscitation at Birth

U

University Hospital Padova

Status

Completed

Conditions

Perinatal Asphyxia

Treatments

Other: Heart rate assessment (stethoscope)
Other: Heart assessment (umbilical cord palpation)

Study type

Interventional

Funder types

Other

Identifiers

NCT03854435
University of Padova

Details and patient eligibility

About

Algorithms for neonatal resuscitation adapted to low resource settings include HR evaluation by auscultation or umbilical cord palpation at about one minute of life.

Previous studies conducted in high resource settings showed that auscultation of the precordium is more accurate than umbilical palpation to assess HR of healthy infants at birth.The last versions of the American Heart Association and the European Resuscitation Council Guidelines on Neonatal resuscitation suggest that "during resuscitation of term and preterm newborns, the use of 3-lead ECG for the rapid and accurate measurement of the newborn's heart rate may be reasonable". However, this remains a weak recommendation with a very-low-quality evidence.

In low resource countries, a stethoscope is rarely available and palpation of the umbilical pulse is the method used for detecting HR. Although this is preferable to other palpation sites (i.e. femo-ral and brachial artery), there is a high likelihood of underestimating HR with palpation of the umbilical pulse in healthy infants.

The accuracy of assessing HR by auscultation and umbilical palpation in newborn infants requir-ing resuscitation remains unknown.

To the investigator's knowledge, there are not previous studies that have compared the accuracy of HR estima-tion by auscultation vs. umbilical palpation in newborn infants needing resuscitation This study was designed to compare two different methods (auscultation and umbilical cord pal-pation) of HR estimation in newborn infants needing resuscitation, in order to determine which method is most suitable for use in clinical practice.

Enrollment

60 patients

Sex

All

Ages

Under 30 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. inborn infants (and)
  2. need for resuscitation (and)
  3. parental consent; a written informed consent will be obtained by a member of the neonatal staff involved in the study from a parent or guardian at maternal admission to the obstetrical ward or prior to delivery.

Exclusion criteria

  1. Major congenital malformations;
  2. Parental refusal to participate to the study.

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Heart rate assessed by using a stethoscope (auscultation)
Experimental group
Description:
Heart rate will be assessed by using a stethoscope (auscultation) in newborn infants immediately after birth
Treatment:
Other: Heart rate assessment (stethoscope)
Heart rate assessed by palpation of the umbilical cord
Active Comparator group
Description:
Heart rate will be assessed by palpation of the umbilical in newborn infants immediately after birth
Treatment:
Other: Heart assessment (umbilical cord palpation)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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