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Time to Accurate Heart Rate on Neonatal Outcomes (GE-EKG)

Primary Purpose

Premature Infant, Extremely Low Birth Weight, Extreme Prematurity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
iRes Warmer with ResusView
iRes Warmer without ResusView
Sponsored by
Sharp HealthCare
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Premature Infant focused on measuring electrocardiogram, Neonatal Resuscitation, resuscitation of premature infants

Eligibility Criteria

23 Weeks - 32 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants who are delivered to mothers over the age of 16 years of age
  • Infants delivered at 23+0 to 32+6 weeks estimated gestational age based on the best obstetric estimate at the time of delivery.
  • Infants without known congenital malformations prior to delivery
  • Antenatal consent

Exclusion Criteria:

  • Infants who are delivered to mothers under the age of 16 years of age
  • Known congenital anomalies of newborn prior to delivery
  • Cardiac defects other than small Ventricular septum defect and Patent ductus arteriosus
  • Multiples
  • Declined consent
  • iRes Warmer with ResusView not available at time of delivery

Sites / Locations

  • Sharp Mary Birch Hospital for Women and Newborns

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

iRes Warmer with ResusView

iRes Warmer without ResusView

Arm Description

iRes Warmer with ResusView program with experimental electrocardiogram monitor will be used for heart rate monitoring in the first 10 minutes of life during routine care and and/or neonatal resuscitation.

An external non-experimental electrocardiogram monitor will be used for heart rate monitoring in the first 10 minutes of life during routine care and and/or neonatal resuscitation.

Outcomes

Primary Outcome Measures

Time to heart rate display in iRes Warmer with Resusview
Measure time from birth to heart rate displayed on monitor following lead placement

Secondary Outcome Measures

Time to first change in Fraction of inspired oxygen
Measure time from birth to first increase or decrease in fraction of inspired oxygen from ECG lead placement
Time to first change in airway pressure
Measure time from birth to first increase or decrease in airway pressure from ECG lead placement
Time to initiation of Positive Pressure Ventilation (PPV)
Measure time from birth to start of PPV following first heart rate display

Full Information

First Posted
October 2, 2020
Last Updated
December 10, 2021
Sponsor
Sharp HealthCare
Collaborators
GE Healthcare, Sharp Mary Birch Hospital for Women & Newborns
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1. Study Identification

Unique Protocol Identification Number
NCT04587934
Brief Title
Time to Accurate Heart Rate on Neonatal Outcomes
Acronym
GE-EKG
Official Title
Time to Accurate Heart Rate on Neonatal Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
June 30, 2021 (Actual)
Study Completion Date
December 10, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sharp HealthCare
Collaborators
GE Healthcare, Sharp Mary Birch Hospital for Women & Newborns

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this trial is to compare the time to first heart rate displayed for iRes Warmer with ResusView and using iRes Warmer without ResusView when used in the resuscitation (e.g. Cardiopulmonary resuscitation or breathing assistance) of premature newborns (23 to 32+6 weeks gestation).
Detailed Description
This is a prospective interventional randomized control trial. Infants born between 23+0 and 32+6 estimated gestational age will be randomized using a computer generate allocation sequence stratified by gestational age. Randomization cards will be placed in opaque envelopes. For the intervention group, the care team will use the Panda iRes Warmer with ResusView Bed during resuscitation interventions in the first 10 minutes of life. During use of the iRes-warmer, standard nursing care of an infant on a radiant warmer will be followed. Participants assigned to the control group will receive interventions using the same model Panda bed without ResusView. There is no minimum time for monitoring, and the maximum time depends on clinical determination for use of heart rate feature for each resuscitation event. Data including the infant's gestational age, Electrocardiogram lead type and activities that occurred during resuscitation will be recorded for the first 10 minutes of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Infant, Extremely Low Birth Weight, Extreme Prematurity
Keywords
electrocardiogram, Neonatal Resuscitation, resuscitation of premature infants

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
iRes Warmer with ResusView
Arm Type
Experimental
Arm Description
iRes Warmer with ResusView program with experimental electrocardiogram monitor will be used for heart rate monitoring in the first 10 minutes of life during routine care and and/or neonatal resuscitation.
Arm Title
iRes Warmer without ResusView
Arm Type
Active Comparator
Arm Description
An external non-experimental electrocardiogram monitor will be used for heart rate monitoring in the first 10 minutes of life during routine care and and/or neonatal resuscitation.
Intervention Type
Device
Intervention Name(s)
iRes Warmer with ResusView
Other Intervention Name(s)
Panda Bed with ECG Feature
Intervention Description
Rapid heart rate display utilizing optimized ECG algorithm in iRes Warmer in babies delivered between 23+0 and 32+6 weeks estimated gestational age
Intervention Type
Other
Intervention Name(s)
iRes Warmer without ResusView
Other Intervention Name(s)
Standard of Care
Intervention Description
Electrocardiogram monitoring using external ECG monitor in babies delivered between 23+0 and 32+6 weeks estimated gestational age
Primary Outcome Measure Information:
Title
Time to heart rate display in iRes Warmer with Resusview
Description
Measure time from birth to heart rate displayed on monitor following lead placement
Time Frame
Birth to 10 minutes of life
Secondary Outcome Measure Information:
Title
Time to first change in Fraction of inspired oxygen
Description
Measure time from birth to first increase or decrease in fraction of inspired oxygen from ECG lead placement
Time Frame
Birth to 10 minutes of life
Title
Time to first change in airway pressure
Description
Measure time from birth to first increase or decrease in airway pressure from ECG lead placement
Time Frame
Birth to 10 minutes of life
Title
Time to initiation of Positive Pressure Ventilation (PPV)
Description
Measure time from birth to start of PPV following first heart rate display
Time Frame
Birth to 10 minutes of life
Other Pre-specified Outcome Measures:
Title
Time of electrode placement
Description
Measure time from birth to application of Electrocardiogram electrodes from time of birth
Time Frame
Birth to 10 minutes of life
Title
Is the rhythm recognized?
Description
Identify if a cardiac rhythm is recognized by Electrocardiogram monitor (Yes/No)
Time Frame
Birth to 10 minutes of life
Title
Time to rhythm recognition
Description
Measure at what time the Warmer displays the baby's cardiac rhythm
Time Frame
Birth to 10 minutes of life

10. Eligibility

Sex
All
Minimum Age & Unit of Time
23 Weeks
Maximum Age & Unit of Time
32 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants who are delivered to mothers over the age of 16 years of age Infants delivered at 23+0 to 32+6 weeks estimated gestational age based on the best obstetric estimate at the time of delivery. Infants without known congenital malformations prior to delivery Antenatal consent Exclusion Criteria: Infants who are delivered to mothers under the age of 16 years of age Known congenital anomalies of newborn prior to delivery Cardiac defects other than small Ventricular septum defect and Patent ductus arteriosus Multiples Declined consent iRes Warmer with ResusView not available at time of delivery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anup Katheria, MD
Organizational Affiliation
Sharp HealthCare
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sharp Mary Birch Hospital for Women and Newborns
City
San Diego
State/Province
California
ZIP/Postal Code
92123
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data, particularly data that underlie the results reported in this article after deidentification will be available with other researchers, including data dictionaries for meta-analysis.
IPD Sharing Time Frame
Beginning 6 months and ending 36 months following article publication
IPD Sharing Access Criteria
Data and publication are available at http://clinicaltrials.gov
IPD Sharing URL
http://clinicaltrials.gov
Citations:
PubMed Identifier
29099872
Citation
Katheria A, Arnell K, Brown M, Hassen K, Maldonado M, Rich W, Finer N. A pilot randomized controlled trial of EKG for neonatal resuscitation. PLoS One. 2017 Nov 3;12(11):e0187730. doi: 10.1371/journal.pone.0187730. eCollection 2017.
Results Reference
background
PubMed Identifier
32102255
Citation
Johnson PA, Schmolzer GM. Heart Rate Assessment during Neonatal Resuscitation. Healthcare (Basel). 2020 Feb 23;8(1):43. doi: 10.3390/healthcare8010043.
Results Reference
background
Citation
Neonatal Resuscitation. Vol. 7th edition. 2016, Elk Grove Village, IL: American Academy of Pediatrics.
Results Reference
background
PubMed Identifier
34715091
Citation
Katheria AC, Morales A, Shashank S, Rich WD, Finer NN. A Pilot Randomized Trial of Heart Rate Monitoring Using Conventional Versus a New Electrocardiogram Algorithm during Neonatal Resuscitation at Birth. J Pediatr. 2022 Mar;242:245-247.e1. doi: 10.1016/j.jpeds.2021.10.037. Epub 2021 Oct 27.
Results Reference
derived

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Time to Accurate Heart Rate on Neonatal Outcomes

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