CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 90 enrolled
Drug / intervention
Forced Air warmer +1 moreprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02990429
NCT02990429N/ACompleted

Comparison Between Forced Air and Intravenous Fluid Warmers in Gynecologic Laparoscopic Surgery

Siriraj Hospital·interventional·Posted Dec 13, 2016·Updated Apr 4, 2019

In Brief

A clinical study evaluating Forced Air warmer and Intravenous Fluid Warmer for Hypothermia; Anesthesia. Completed, enrolled 90 participants across 1 site.

Detailed Summary

Perioperative hypothermia is a common problem. It has been defined as a core temperature below 36ºC. The reasons why patient undergoing gynecologic laparoscopic surgery has perioperative hypothermia because the reduced metabolic heat production, redistribution of heat from the core to the periphery and impaired thermoregulation (due to anesthetics), use of cool carbon dioxide gas insufflations and surgical irrigation solution, as well as heat loss due to the cool environment. This perioperative problem has been linked to adverse patient outcomes such as myocardial ischemia as hypothermia increases plasma catecholamine, surgical site infection as hypothermia diminishes wound tissue O2 tension and coagulopathy as hypothermia impairs platelet function. It claims that perioperative heat loss occurs by radiation (60%), convection (25%) and evaporation (10%). This is caused by the difference between peripheral body and ambient temperature, air circulation around the body and vasodilatation. In daily practice, most anesthesia personnel warm patient peri-operatively by using force air warmer and intravenous fluid warmer. This study aimed to compare the difference of core and room temperature in patients undergoing gynecologic laparoscopic surgery by using forced air and intravenous fluid warmer

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesThailand
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedDec 13, 2016
Enrollment StartApr 1, 2016
Primary CompletionDec 1, 2018
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 9.6 years ago

Interventions

Forced Air warmerprocedure

* record room temperature * record core temperature (tympanic membrane) * General anesthesia * using forced air warmer (bair hugger) * Intravenous fluid at room temperature * room temperature and core temperature q15 minutes * anesthesia finish, stop bair hugger * record core temperature before recovery room

Intravenous Fluid Warmerprocedure

* record room temperature * record core temperature (tympanic membrane) * General anesthesia * using ranger warmer * Intravenous fluid at room temperature * room temperature and core temperature q15 minutes * anesthesia finish, stop ranger warmer * record core temperature before recovery room