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Evaluation of Use of Plastic Bags to Prevent Neonatal Hypothermia-Part III

Randomized Evaluation of the Use of Plastic Bags to Prevent Neonatal Hypothermia in Developing Countries-Part III

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01604434
Enrollment
0
Registered
2012-05-23
Start date
2012-06-30
Completion date
2019-10-31
Last updated
2019-02-20

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

Conditions

Hypothermia

Keywords

Hypothermia, Low birth Weight, Newborn, Incubator, Plastic bag

Brief summary

The overall hypothesis is that plastic bags used in combination with WHO thermoregulation care will reduce the incidence of hypothermia in preterm/low birth weight and full term infants when compared to routine WHO thermoregulation care alone. Part III is for preterm/low birth weight infants with or without a plastic torso wrap during the first hour after birth to assist with temperature regulation during placement in an incubator.

Detailed description

Incubators in the developing world often lack humidifiers. The resting dry heat increases evaporative heat loss, the most prominent form of heat loss in premature infants due to their increased body surface area and immature stratum corneum. By potentially increasing humidity around the infants and decreasing evaporative heat losses, plastic bags may improve incubator warming. This study will compare the incidence of hypothermia in infants placed in an incubator for at least one hour randomized to receive standard incubator protocol (control group) or standard incubator protocol plus a plastic bag covering their torsos and lower extremities (intervention group). The axillary temperature of each infant will be taken before placement into the incubator and one hour later when the bag will be removed. Blood pressure, blood sugar, seizures, weight gain, hyperthermia, death, observation for respiratory distress syndrome, bronchopulmonary dysplasia, pneumothorax, sepsis, intraventricular hemorrhage, periventricular leukomalacia, necrotizing enterocolitis, intestinal perforation, pulmonary hemorrhage, incubator temperature, and humidity, and length of time in an incubator will be recorded throughout the hospitalization for all infants. With an estimated baseline hypothermia rate of 90% and a hypothesized 20% absolute risk reduction (22% relative risk reduction), a sample size of 118 will be used to have a power of 80% and a confidence interval of 95%.

Interventions

PROCEDUREIncubator-torso bag

While being placed into an incubator, infant will be placed into a plastic bag to his/her axillae and the bag will be folded and taped to itself to prevent it from covering the infant's nose or mouth. The infant will be wrapped in a blanket over the plastic bag and will receive a cloth hat. He/she will remain in the bag for one hour.

PROCEDUREIncubator-no plastic bag

Infant will be placed in the incubator, wrapped in a blanket, with a cloth hat, according to standard protocol.

Sponsors

Children's Health System, Alabama
CollaboratorOTHER
University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Minutes to 72 Hours
Healthy volunteers
No

Inclusion criteria

* Infant admitted to the NICU * Current weight between 1,000 and 2,500g * Being placed in an incubator

Exclusion criteria

* Abdominal wall defect or myelomeningocele * Major congenital anomalies * Blistering skin disorder

Design outcomes

Primary

MeasureTime frameDescription
Axillary temperature 36.5-37.5 degrees Celsius1-72 hoursTemperature taken per axilla for 1 minute

Secondary

MeasureTime frameDescription
Blood glucoseUp to 4 weeksMeasure of blood glucose per laboratory value taken per heel stick
SeizureUp to 4 weeksSeizure activity diagnosed by medical doctor or nurse. No electroencephalogram will be done.
Weight gainUp to 4 weeksInfant will be weighed daily and rates of weight gain will be calculated
Respiratory Distress Syndrome (RDS) Respiratory Distress Syndrome (RDS)Up to 4 weeksDocumentation of increased work of breathing, retractions, and a need for oxygen, intubation, or surfactant
Bronchopulmonary dysplasia (BPD)28 days after birthOxygen requirement at 28 days after birth
PneumothoraxUp to 4 weeksEither chest radiograph documentation or clinical deterioration consistent with air leak
SepsisUp to 4 weeksCulture proven or culture negative clinically treated course consistent with sepsis
Blood PressureUp to 4 weeksMeasure of extremity blood pressure per cuff taken during nursery stay
Necrotizing enterocolitis or intestinal perforationUp to 4 weeksDocumentation of pneumatosis or intestinal perforation on x-ray or treatment course for clinical necrotizing enterocoliities per Bell's Classification stage greater than 1.
Pulmonary hemorrhageUp to 4 weeksBlood seen in the endotracheal tube and treated by physician
DeathUp to 4 weeksCardiorespiratory failure
HyperthermiaUp to 4 weeksAxillary temperature \> 38 degrees Celsius per temperature taken per axilla for one minute
Length of time in IncubatorUp to 4 weeksDocumentation of length of time spent in incubator and number of times placed in incubator
Temperature and humidity1 hourA recording of the air temperature and humidity within the incubator will be obtained with each axillary temperature measurement
Major brain injuryUp to 4 weeksIntracranial hemorrhage grade 3-4 or periventricular leukomalacia documented on cranial ultrasound

Countries

Zambia

Outcome results

None listed

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