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Hypothermia and the Effect of Ambient Temperature 2 (HEAT2)

Primary Purpose

Hypothermia, Neonatal Outcome, Cesarean Section

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Change in ambient operating room temperature
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypothermia

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts 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.

Sites / Locations

  • Parkland Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Ambient operating room temperature of 67°F

Ambient operating room temperature of 75°F

Arm Description

These patients will have an operating room temperature of 67°F for cesarean delivery, the standard of care at our institution.

Intervention: Ambient operating room temperature of 75°F for cesarean delivery, which is closer to World Health Organization recommendations.

Outcomes

Primary Outcome Measures

Neonatal Composite Morbidities
Need for respiratory support, Hypoglycemia necessitating treatment, Culture-proven sepsis; Mortality

Secondary Outcome Measures

Maternal Recovery Room Dwell Times after Cesarean
Maternal Hypothermia
An oral temperature of less than 36.5C

Full Information

First Posted
December 28, 2016
Last Updated
October 10, 2018
Sponsor
University of Texas Southwestern Medical Center
Collaborators
Parkland Health and Hospital System
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1. Study Identification

Unique Protocol Identification Number
NCT03008577
Brief Title
Hypothermia and the Effect of Ambient Temperature 2
Acronym
HEAT2
Official Title
The Impact of Ambient Cesarean Room Temperature on Neonatal Morbidity
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
August 2016 (undefined)
Primary Completion Date
May 2018 (Actual)
Study Completion Date
May 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Texas Southwestern Medical Center
Collaborators
Parkland Health and Hospital System

4. Oversight

5. Study Description

Brief Summary
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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypothermia, Neonatal Outcome, Cesarean Section

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
5221 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ambient operating room temperature of 67°F
Arm Type
No Intervention
Arm Description
These patients will have an operating room temperature of 67°F for cesarean delivery, the standard of care at our institution.
Arm Title
Ambient operating room temperature of 75°F
Arm Type
Active Comparator
Arm Description
Intervention: Ambient operating room temperature of 75°F for cesarean delivery, which is closer to World Health Organization recommendations.
Intervention Type
Other
Intervention Name(s)
Change in ambient operating room temperature
Primary Outcome Measure Information:
Title
Neonatal Composite Morbidities
Description
Need for respiratory support, Hypoglycemia necessitating treatment, Culture-proven sepsis; Mortality
Time Frame
Up to 24 hours following delivery
Secondary Outcome Measure Information:
Title
Maternal Recovery Room Dwell Times after Cesarean
Time Frame
Up to 48h following delivery
Title
Maternal Hypothermia
Description
An oral temperature of less than 36.5C
Time Frame
Up to 24 hours after delivery

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Facility Information:
Facility Name
Parkland Memorial Hospital
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States

12. IPD Sharing Statement

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Hypothermia and the Effect of Ambient Temperature 2

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