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Hypothermia and the Effect of Ambient Temperature 2 (HEAT2)

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Cesarean Section
Neonatal Outcome
Hypothermia

Treatments

Other: Change in ambient operating room temperature

Study type

Interventional

Funder types

Other

Identifiers

NCT03008577
STU 062016-040

Details and patient eligibility

About

Neonatal hypothermia is associated with increased risk of mortality as well as multiple morbidities. The prior HEAT study conducted at our institution showed a difference in neonatal hypothermia with a change in ambient operating room temperature. The investigator's objective is to determine if an increase in ambient operative room temperature decreases the rate of neonatal morbidity. Operating room temperature will be randomized to the current institutional standard of 20°C (67°F) or a temperature of 24°C (75°F), on a weekly basis for a period of 1.2 years.

Full description

This is an open, prospective, randomized, single center trial that will address the primary research question: Does an increase in ambient operating room temperature result in a lower rate of composite neonatal morbidities? During the 1.2 year study period, the operating room temperatures on labor and delivery will be adjusted to either the current standard of care with ambient operating room temperature of 20°C (67°F), or the maximum temperature allowable per hospital policy in the current operating rooms, which is 24°C (75°F), as determined by cluster randomization. Composite neonatal morbidities will be recorded including hypoglycemia necessitating treatment; need for respiratory support within the first 24 hours; culture-proven sepsis; and mortality. Association of outcomes with the types of passive and active warming performed will include these morbidities stratified by gestational age as well as maternal outcomes. In addition, an electronic survey will be administered to the operating resident physicians to assess their experience with the study conditions.

Enrollment

5,221 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All pregnant women and their neonates undergoing cesarean delivery by the Parkland Hospital Obstetrics Service on the Labor and Delivery unit during the study period.

Exclusion criteria

  • Exclusion criteria include cases where a cesarean delivery is planned but a precipitous vaginal delivery occurs, intrauterine fetal demise has been diagnosed prior to start of surgery, the neonate is noted to have a major congenital anomaly and resuscitative efforts are not performed ("comfort care only" provided), or a neonatal temperature is not available.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

5,221 participants in 2 patient groups

Ambient operating room temperature of 67°F
No Intervention group
Description:
These patients will have an operating room temperature of 67°F for cesarean delivery, the standard of care at our institution.
Ambient operating room temperature of 75°F
Active Comparator group
Description:
Intervention: Ambient operating room temperature of 75°F for cesarean delivery, which is closer to World Health Organization recommendations.
Treatment:
Other: Change in ambient operating room temperature

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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