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Effect of Drying Before Plastic Wrapping on Thermal Losses in Very Preterm Infants at Birth

Effect of Drying Before Plastic Wrapping on Thermal Losses in Very Preterm Infants at Birth: a Multicenter, Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05740072
Acronym
NEODRY
Enrollment
346
Registered
2023-02-22
Start date
2023-02-28
Completion date
2023-10-31
Last updated
2023-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Temperature Regulation; Disorder, Fetus or Newborn

Keywords

Newborn, Prematurity, Temperature, Delivery

Brief summary

This is a multicenter, unblinded, randomized controlled trial comparing drying vs. not drying before plastic wrapping for the thermoregulation of very preterm infants at birth. The aim of this study will be to compare two modes of thermal management (plastic wrapping with or without drying) for preventing heat loss at birth in very preterm infants.

Detailed description

Background: 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. While drying is recommended for the thermal management of infants with gestational age \>32 weeks, this procedure is not indicated for very preterm infants who should be put in a plastic wrap immediately at birth without drying. However, such indication is based on studies comparing wrapping without drying vs. drying without wrapping, while the potential advantages of combining these interventions were not explored. We hypothesized that drying before wrapping could prevent heat loss immediately after birth and reduce hypothermia at NICU admission in very preterm infants. Objective: The aim of this study will be to compare two modes of thermal management (plastic wrapping with or without drying) for preventing heat loss at birth in very preterm infants. Methods: This is a multicenter, unblinded, randomized controlled trial comparing drying vs. not drying before plastic wrapping for the thermoregulation of very preterm infants at birth. After obtaining parental consent, all infants with estimated birth weight \<1500 g and/or gestational age ≤30+6 weeks will be assigned to be managed with or without drying before plastic wrapping. Room temperature and maternal temperature will be measured at the time of delivery. Patients allocated in both groups will be managed based on the current guidelines for neonatal resuscitation. The primary outcome measure will be the proportion of neonates in the normal thermal range (temperature 36.5-37.5°C) at NICU admission. Secondary outcome measures will be: proportion of neonates with hypothermia (\<36.5°C and \<36.0°C) at NICU admission; proportion of hyperthermic neonates (temperature \>37.5°C) at NICU admission; temperature at 1 hour after NICU admission; proportion of intraventricular hemorrhage; proportion of respiratory distress syndrome; proportion of late onset sepsis; proportion of bronchopulmonary dysplasia; mortality before hospital discharge.

Interventions

OTHERDrying before wrapping

Immediately after birth, the infant's body will be dried before wrapping in a plastic bag

OTHERNo drying before wrapping

Immediately after birth, the infant will be put in a plastic bag without wrapping

Sponsors

University Hospital Padova
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
0 Minutes to 6 Months
Healthy volunteers
Yes

Inclusion criteria

* Estimated birth weight \<1500 g and/or gestational age ≤30+6 weeks (and) * Inborn (and) * Parental consent; written informed consent will be obtained by a member of the neonatal team involved in the study from a parent or guardian at the maternal admission to the Obstetric Department.

Exclusion criteria

* Major congenital malformations (i.e. cardiac disease, defects of abdominal wall, ...); * Outborn; * Parental refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
Number (percentage) of neonates in the normal thermal range (temperature 36.5-37.5°C) at Neonatal Intensive Care Unit admission.25 minutes

Secondary

MeasureTime frameDescription
Number (percentage) of neonates with moderate-severe hypothermia (temperature <36.0°C) at neonatal intensive care unit admission25 minutes
Number (percentage) of neonates hyperthermia (temperature >37.5°C) at NICU admission at neonatal intensive care unit admission25 minutes
Temperature at 1 hour after neonatal intensive care unit admission60 minutesAxillary temperature will be registered at 1 hour after neonatal intensive care unit admission
Number (percentage) of infants with intraventricular hemorrhage (all grades and grade III-IV)10 daysThe grade of intraventricular hemorrhage will be defined on Levine classification
Number (percentage) of neonates with hypothermia (temperature <36.5°C) at neonatal intensive care unit admission25 minutes
Number (percentage) of infants with late-onset sepsis7 daysSespsis will be defined based on the presence of a positive blood colture 72 hours after birth
Number (percentage) of infants with bronchopulmonary dysplasia36 postnatal weeksBronchopulmonary dysplasia will be defined as the need for oxygen at 36 postnatal weeks gestation
Number (percentage) of infants died before hospital discharge5 months
Number (percentage) of infants with respiratory distress syndrome72 hoursRespiratory distress syndrome will be defined as presence of clinical signs of respiratory distress and radiological findings

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026