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Temperature Study in Cesarean Section
Not Recruiting
Trial ID: NCT01249014
Purpose
During surgery body temperature can decrease which can adversely affect how people recover
from surgery. This is a common problem. We aim to reduce the incidence of this drop in body
temperature during surgery by testing the effectiveness of warm intravenous fluids that the
patients will receive as they are being infused, and of warm air blown into a blanket
covering the body. The control group will not have any active warming methods.
Study group 1 will have the intravenous fluid warmer in the pre- and intraoperative period.
Study group 2 will have a forced-air warmer in the intra-operative period as well as the
fluid warmer in the pre- and intraoperative period. We will also observe the neonates' vital
signs following delivery.
Official Title
Study Using Fluid Warming and Forced Air Warming Immediately Prior to and During Elective Cesarean Section
Eligibility
Inclusion Criteria:18-40 years. Healthy term (> 37 weeks) pregnant patients undergoing
elective cesarean section with spinal anesthesia.
We will not discriminate with regard to ethnic background. ASA 1 and 2 patients scheduled
for elective cesarean sections under spinal anesthesia at LPCH.
Exclusion Criteria:Not ASA 1 or 2 Not spinal anesthetic
Intervention(s):
other: Warmed fluids
other: Fluid warmer and warming blanket
device: Belmont fluid warmer
device: Bair hugger warming blanket
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Pervez Sultan, MBChB, FRCA
650-526-8414