Hypothermia Clinical Trial
Official title:
Randomized, Prospective Study to Determine the Effects of Pre-warming on OR Patient Temperatures and Perioperative Surgical Outcomes
Verified date | August 2016 |
Source | 3M |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Interventional |
The application of active warming to patients whether awake or under general anesthesia has
been proven safe in numerous studies and it is common practice to use warmers. The warmers
are commonly used with both the supplied blankets and also with hospital blankets.
Subjects receiving standard care will not benefit from this study. Subjects in the
investigational group may benefit in several ways:
- Increased comfort in the pre-operative period by being warmer
- Decreased incidence of mild hypothermia
- Possible decreased incidence of transfusion with less bleeding
- Possible decreased pain and discomfort in the Post-Anesthesia Care Unit (PACU)
- Possible shorter stay in the PACU and overall Length of Stay (LOS)
- Possible decreased risk for surgical site infection
Status | Completed |
Enrollment | 220 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 19 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Elective or "urgent" surgery under general anesthesia - =19 years but =85 years of age - Able to provide informed consent. Exclusion Criteria: - Refusal of Informed consent - Metabolic derangement/drug therapy already affecting thermal homeostasis - Preexisting hypothermia (<35.5 degreeC) or hyperthermia (>37.5 degreeC) (oral) - Surgical procedure anticipated to be longer than 6 hours or less than 1 hour - Emergency (category 1a) Surgery - Patients undergoing exclusively spinal or epidural anesthesia - Patients receiving aortic cross-clamping - Patients receiving transdermal medications |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Canada | Royal Columbian Hospital | Vancouver | British Columbia |
Lead Sponsor | Collaborator |
---|---|
3M |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Duration of hypothermia | The primary endpoint is duration of hypothermia as measured by the area under the curve (AUC). This is achieved by recording patient temperature readings continuously from baseline (prior to initiation of 30 minutes if active or passive pre-warming) until PACU discharge. | Up to 12 hours, until PACU discharge | Yes |
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