Effect of a Servo-control System on Heat Loss in Very Low Birth Weight Infants at Birth (SCOPRI)
Primary Purpose
Neonatal Hypothermia
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Thermal servo-controlled system
Sponsored by
About this trial
This is an interventional prevention trial for Neonatal Hypothermia
Eligibility Criteria
Inclusion Criteria:
- Estimated birth weight <1500 g and/or gestational age <30+6 weeks (and)
- Inborn (and)
- Parental consent
Exclusion Criteria:
- Major congenital malformations (i.e. cardiac disease, defects of abdominal wall, ...);
- Outborn;
- Parental refusal to participate to the study.
Sites / Locations
- University of Padova
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Servo-controlled system
No servo-controlled system
Arm Description
The temperature probe of the servo-controlled system will be positioned on the patient's abdomen with an adhesive tape. The body temperature will be set at 37°C.
The temperature of the infant warmer will be manually set at maximum of power output.
Outcomes
Primary Outcome Measures
Proportion of neonates in the normal thermal range (temperature 36.5-37.5°C) at NICU admission
Secondary Outcome Measures
Proportion of neonates with temperature less than 36.0°C at NICU admission
Proportion of neonates with mild hypothermia (temperature 36.0-36.4°C) at NICU admission
Proportion of hyperthermic neonates (temperature >38.0°C) at NICU admission
Temperature at 1 hour after NICU admission
Proportion of ineonates with ntraventricular hemorrhage (grade I-IV)
Propoertions of neoantes with respiratory distress syndrome
Proportion of neonates with late onset sepsis
Proportion of neonates with bronchopulmonary dysplasia
Proportion of deaths
Full Information
NCT ID
NCT03844204
First Posted
February 14, 2019
Last Updated
April 2, 2020
Sponsor
University Hospital Padova
1. Study Identification
Unique Protocol Identification Number
NCT03844204
Brief Title
Effect of a Servo-control System on Heat Loss in Very Low Birth Weight Infants at Birth
Acronym
SCOPRI
Official Title
Effect of a Servo-control System on Heat Loss in Very Low Birth Weight Infants at Birth: a Multicenter, Prospective, Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
March 1, 2019 (Actual)
Primary Completion Date
February 29, 2020 (Actual)
Study Completion Date
February 29, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Padova
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Hypothermia in preterm infants during the immediate postnatal phase is associated with morbidity and mortality and remains an unresolved, worldwide challenge.
A list of interventions, including adequate room temperature, use of infant warmers, polyethylene bags/wrap, pre-heated mattresses, caps and heated and humidified gases, to prevent thermal loss at birth in very preterm infants has been recommended, but a certain percentage of very preterm infants are hypothermic at the time of the neonatal intensive care unit (NICU) admission suggesting that further measures are needed. The thermal servo-controlled systems are routinely used in the NICU to accurately manage the patients' temperature, but their role during the immediate postnatal phase has not been previously assessed.
We hypothesized that using a thermal servo-control system at delivery could prevent heat loss during this delicate phase and increase the percentage of very low birth weight infants (VLBWI) in the normal thermal range (temperature 36.5-37.5°C) at NICU admission. The aim of this study will be to compare two modes of thermal management (with and without the use of a thermal servo-controlled system) for preventing heat loss at birth in VLBWI infants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal Hypothermia
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Nurses who will measure the temperature at NICU admission are blind to treatment arm in the delivery room
Allocation
Randomized
Enrollment
440 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Servo-controlled system
Arm Type
Experimental
Arm Description
The temperature probe of the servo-controlled system will be positioned on the patient's abdomen with an adhesive tape. The body temperature will be set at 37°C.
Arm Title
No servo-controlled system
Arm Type
Active Comparator
Arm Description
The temperature of the infant warmer will be manually set at maximum of power output.
Intervention Type
Device
Intervention Name(s)
Thermal servo-controlled system
Intervention Description
All patients will be positioned under the infant warmer. In the treatment group, a probe positioned on the skin of the neonate will guide the thermal exposure in a servo-controlled modality. In the control group, thermal exposure will be determined manually by setting the power of the heater at the maximum output.
Primary Outcome Measure Information:
Title
Proportion of neonates in the normal thermal range (temperature 36.5-37.5°C) at NICU admission
Time Frame
30 minutes
Secondary Outcome Measure Information:
Title
Proportion of neonates with temperature less than 36.0°C at NICU admission
Time Frame
30 minutes
Title
Proportion of neonates with mild hypothermia (temperature 36.0-36.4°C) at NICU admission
Time Frame
30 minutes
Title
Proportion of hyperthermic neonates (temperature >38.0°C) at NICU admission
Time Frame
30 minutes
Title
Temperature at 1 hour after NICU admission
Time Frame
1 hour
Title
Proportion of ineonates with ntraventricular hemorrhage (grade I-IV)
Time Frame
7 days
Title
Propoertions of neoantes with respiratory distress syndrome
Time Frame
3 days
Title
Proportion of neonates with late onset sepsis
Time Frame
14 days
Title
Proportion of neonates with bronchopulmonary dysplasia
Time Frame
36 gestational weeks
Title
Proportion of deaths
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Minute
Maximum Age & Unit of Time
1 Minute
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Estimated birth weight <1500 g and/or gestational age <30+6 weeks (and)
Inborn (and)
Parental consent
Exclusion Criteria:
Major congenital malformations (i.e. cardiac disease, defects of abdominal wall, ...);
Outborn;
Parental refusal to participate to the study.
Facility Information:
Facility Name
University of Padova
City
Padova
ZIP/Postal Code
35128
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
33597230
Citation
Cavallin F, Doglioni N, Allodi A, Battajon N, Vedovato S, Capasso L, Gitto E, Laforgia N, Paviotti G, Capretti MG, Gizzi C, Villani PE, Biban P, Pratesi S, Lista G, Ciralli F, Soffiati M, Staffler A, Baraldi E, Trevisanuto D; Servo COntrol for PReterm Infants (SCOPRI) Trial Group. Thermal management with and without servo-controlled system in preterm infants immediately after birth: a multicentre, randomised controlled study. Arch Dis Child Fetal Neonatal Ed. 2021 Nov;106(6):572-577. doi: 10.1136/archdischild-2020-320567. Epub 2021 Feb 17.
Results Reference
derived
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Effect of a Servo-control System on Heat Loss in Very Low Birth Weight Infants at Birth
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