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RECRUITING
NCT05015582
NA

Perioperative Warming Measures in Cesarean Delivery

Sponsor: The University of Texas Health Science Center, Houston

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate the best method for keeping patients warm during cesarean deliveries and the effect of temperature change on the patient and baby

Official title: Randomized Control Trial Assessing Effectiveness of Perioperative Warming Measures in Parturients Undergoing Cesarean Delivery

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2021-08-23

Completion Date

2023-08-01

Last Updated

2023-01-10

Healthy Volunteers

No

Interventions

DEVICE

Pre op upper body forced air warming (32˚C)

Use of upper body forced air warming at ambient (32˚C) for at least 30 minutes

DEVICE

Pre op lower body forced air warming (32˚C)

lower body forced air warming at ambient (32˚C) for at least 30 minutes

DEVICE

Pre op fluids (45˚C)

fluids from warmed cabinet set at 45˚C

DEVICE

Intra op upper body forced air warming (32˚C)

Use of upper body forced air warming intra-operative at ambient (32˚C)

DEVICE

Intra op fluids at room temperature

IV fluids at room temperature

DEVICE

Intra op upper body forced air warming at (32˚C)

upper body forced air warming intra-operative at ambient (32˚C)

DEVICE

Intra op upper body forced air warming at (42˚C)

upper body forced air warming intra-operative at ambient (42˚C)

DEVICE

Intra op lower body forced air warming at (32˚C)

Lower body forced air warming intra-operative at ambient (32˚C)

DEVICE

Intra op lower body forced air warming at (42˚C)

Lower body forced air warming intra-operative at ambient (42˚C)

DEVICE

Intra op fluid (42˚C)

IV fluids with hotline fluid warmer set at 42˚C

Locations (1)

The University of Texas Health Science Center at Houston

Houston, Texas, United States