Clinical Trials Directory

Trials / Completed

CompletedNCT02467777

Comparison of Forced Air and Conductive Patient Heating Systems During Ambulatory Surgeries

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Fox Valley Orthopedic Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Comparison of forced air and conductive warming devices in outpatient orthopaedic surgeries.

Detailed description

Patients will be randomized into either the Forced Air group (FA) or Conductive Heat group (CH). Randomization will be based on computer-generated codes that will be maintained in sequentially numbered opaque envelopes. Fifty patients will be recruited with 25 patients being randomized into each group. In patients assigned to the FA group, a Bair Hugger (Arizant Medical, Inc., Eden Prairie, Minnesota) forced-air cover will be positioned over the upper body (if lower extremity surgery) or lower body (if upper extremity surgery). The forced-air blower will be set and activated per standard practice usually after prepping and draping. In patients assigned to the CH group, a VitaHeat (VitaHeat, Inc, Aurora, IL) conductive heating device will be placed under the torso of the patient. The device will be set and activated per standard practice usually just after positioning of the patient on the operating table. Patients in both groups will be otherwise draped per surgical routine. Ambient temperature will be maintained near 20°C. Temperatures will be recorded using a temporal artery thermometer.

Conditions

Interventions

TypeNameDescription
DEVICEBair Hugger
DEVICEVitaHeat

Timeline

Start date
2015-06-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2015-06-10
Last updated
2017-05-11
Results posted
2017-03-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02467777. Inclusion in this directory is not an endorsement.