Clinical Trials Logo

Hypothermia; Anesthesia clinical trials

View clinical trials related to Hypothermia; Anesthesia.

Filter by:
  • Recruiting  
  • Page 1

NCT ID: NCT05349734 Recruiting - Clinical trials for Hypothermia; Anesthesia

Comparison of Underbody and Overbody Forced Air Blanket in Pediatric Patients Undergoing Cardiovascular Interventions

Start date: May 12, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to compare the underbody blanket and overbody blanket for forced air warming to maintain normothermia in pediatric patients undergoing cardiovascular interventions under general anesthesia.

NCT ID: NCT05015582 Recruiting - Clinical trials for Hypothermia; Anesthesia

Perioperative Warming Measures in Cesarean Delivery

Start date: August 23, 2021
Phase: N/A
Study type: Interventional

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

NCT ID: NCT04410068 Recruiting - Clinical trials for Temperature Change, Body

Comparison of Electric Heating Pad Versus Forced-air Warming to Prevent Inadvertent Perioperative Hypothermia

Start date: December 23, 2019
Phase: N/A
Study type: Interventional

Compare core body temperature after laparoscopic surgery using the forced air heating system versus the WARMTAC® (a carbon fiber electric blanket).

NCT ID: NCT03473470 Recruiting - Clinical trials for Hypothermia; Anesthesia

Evaluation of the Active Warming Effects on Maternal and Neonatal Outcome During Cesarean Delivery

Start date: December 22, 2016
Phase: N/A
Study type: Interventional

A prospective randomized study of healthy term parturients undergoing cesarean delivery was designed to assess the impact of the active warming on perioperative and postoperative temperature. The main objective is to evaluate the maternal core temperature in the perioperative and postoperative period during cesarean delivery. The secondary objectives are to assess the incidence of maternal hypothermia, the incidence of maternal shivers, the evaluation of maternal thermal comfort, the neonatal temperature at birth, the Apgar score at 1 and 5 minutes, the umbilical pH, the evaluation of coagulative assessment in case of maternal hypothermia trough the use of thromboelastography. The patients are randomized into three groups: a group of no warmed patients, a second group of Active waming patients with iv fluids and lower body forced air warming and a third group of Active warming patients with only warmed iv fluids. The inclusion criteria are healthy parturients up to age 18. The exclusion criteria included parturients who develop fever, diabetes mellitus, BMI up to 40kg/ m2, coagulative disorders, pre eclampsia or eclampsia, all the factors that can cause intraoperative bleeding such as placental abruption or antecedent placenta overgrowth ( placenta previa).