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Determination of Core Body Temperature in Parturient Warmed With Upper or Underbody Forced Air Cover (Bair Hugger)

Determination of Core Body Temperature in Parturient Warmed With Upper or Underbody Forced Air Cover (Bair Hugger)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05314075
Enrollment
124
Registered
2022-04-06
Start date
2022-12-27
Completion date
2025-07-30
Last updated
2025-09-02

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

Conditions

Cesarean Section

Keywords

Thermoregulation, Forced air warming, upper or lower body forced air cover, core body temperature

Brief summary

This study is intended to calculate the core body temperature in patients who are having a Cesarean Section (C/S) and are kept warm with an Upper Body Forced Air Warming device (Bair Hugger) or underbody forced air warmer. These warming devices are approved and are a required item in many if not all surgical procedures. They are used daily throughout the hospital. The research question is: Where is the best place to position the warming blanket in pregnant mothers undergoing Cesarean section delivery. The researchers hope to compare post - operative core body temperatures in patients getting an Upper Body forced air device versus those getting an Underbody Body forced air warming device.

Interventions

PROCEDUREUpper Body Forced Air Warming device

Patients will have the Bair Hugger placed over the body

PROCEDUREUnder Body Forced Air Warming device

Patients will have the Bair Hugger placed under the body

Sponsors

Virginia Commonwealth University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age =/\> 18 years * Elective non-emergent C-section

Exclusion criteria

* BMI\<18/\>40 * Bleeding Disorders e.g. hemophilia, coagulation abnormality, clotting disorders, bleeding diathesis * Perioperative hemorrhage \>1500ml * Non-Singleton Pregnancies * Complicated Pregnancy (e.g. Eclampsia, Pre-eclampsia) * Conversion to Emergency C-section * Endocrine Pathology- e.g. Thyroid Disease, Insulin Dependent Diabetes * Inmates

Design outcomes

Primary

MeasureTime frameDescription
Core body temperature1 hour post surgeryMaternal core temperatures will be measured using a temperature sensing Foley catheter

Countries

United States

Outcome results

None listed

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