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