The purpose of this study is to see if the combination of a circulating water mattress beneath the patient combined with forced air warming over top of the patient will prevent hypothermia (low body temperature) just as well as a garment that circulates warm water around the patient, during your major abdominal surgery. Patients will be randomly assigned to one of these two groups.
Group A: This group will receive the circulating water garment Group B: This group will receive the circulating water mattress and be covered by a forced air warming device for both the upper body and lower body Once the patient is moved to the operating room table, the surface of the back will begin to be warmed using either the circulating-water garment for those in Group A or the circulating-water mattress for those in Group B. Following the start of anesthesia, additional warming will be done by covering the large parts of the legs and the upper and side of the chest using either the circulating-water garment for those in Group A or upper- and lower-body forced-air warmers for those in Group B. Patient involvement will last until the warming devices are removed prior to departure from the operating room. There is no follow-up to this study.
Study Type
OBSERVATIONAL
Enrollment
50
Cleveland Clinic
Cleveland, Ohio, United States
The primary outcome will comprise the difference between the pre-induction temperature and the intraoperative temperature
Time frame: Every 15 minutes throughout surgery
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