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Intraoperative Warming Comparison of Devices

Primary Purpose

Hypothermia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dynatherm Medical vitalHEAT Temperature Management System vH2
Bair Hugger™ (Arizant Healthcare, Eden Prairie, MN)
Sponsored by
University of South Florida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypothermia focused on measuring intraoperative warming, anesthesia, hypothermia, body temperature

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients undergoing elective open abdominal surgical procedures with an expected duration of 2 to 4 hours and requiring general anesthesia
  • American Society of Anesthesiologists(ASA) physical status I-III
  • Patient age: > 18 years and <80 years

Exclusion Criteria:

  • Patient age: < 18 years and >80 years
  • Patients with break in skin integrity on the extremity selected as the application site
  • Patients with history of upper extremity peripheral vascular disease
  • Patients with history of allergic skin conditions of the upper extremities
  • Patients with history of bleeding disorders/coagulopathy
  • Patient with history of malignant hyperthermia
  • Patients who are pregnant
  • Patient unwilling or unable to give informed consent

Sites / Locations

  • Tampa General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

vH2 System Group

Control Group

Arm Description

The vital heat vH2 system consists of a Control Unit containing the heating system and the vacuum generation pump which connects via an umbilical containing the fluid and vacuum tubing to the Warming Sleeve. The Control Unit also contains the user interface and alarm management systems. The disposable Warming Sleeve consists of a manifold attached to the warming pads and a polyurethane pouch (Vacuum Sleeve) that are placed over the patient's hand and forearm and secured with tape. The Warming Sleeve manifold contains connectors for the fluid and vacuum tubing contained in the umbilical. The vital heat vH2 System will be used for patient warming during these surgical procedures. Monitoring of core temperature via esophageal probe will be done for the purpose of data collection.

The Bair Hugger system is the current standard of care at Tampa General Hospital. It consists of a Temperature Management Unit that contains the heating element, the air circulating motor and the temperature control mechanisms. This unit connects via a hose to the operating room blankets. The Bair Hugger technology relies on heated air convection. Warm air is circulated evenly through the air space in the specially designed blanket, warming the skin surface as well as any insulating blankets placed over the Bair Hugger blanket. The Bair Hugger System is the site's current approach to patient warming during these surgical procedures. Monitoring of core temperature via esophageal probe will be done for the purpose of data collection.

Outcomes

Primary Outcome Measures

Percent of Patients With an Average Intraoperative Temperature Greater Than or Equal to 36 Celcius
Percent of Subjects With an Initial PACU Sublingual Temperature of ≥ 36º C.
Percentage of Patients With a Post Operative Sublingual Temperature Above 36 Degrees Celcius
Percent of subjects with an initial post anesthesia care unit sublingual temperature of ≥ 36º C

Secondary Outcome Measures

Comparison of the Core Body Temperatures at 60 Minutes Post Anesthesia Induction,as Assessed by Esophageal Probe.
Average core body temperature measured with an esophageal probe at 60 minutes post-induction
Average Intraoperative Esophageal Temperature
Average esophageal temperature for the first 70 minutes of surgery following induction of anesthesia.
Median Post Anesthesia Care Unit Sublingual Temperature

Full Information

First Posted
March 27, 2008
Last Updated
September 25, 2012
Sponsor
University of South Florida
Collaborators
Dynatherm Medical Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00650260
Brief Title
Intraoperative Warming Comparison of Devices
Official Title
Intraoperative Warming : Comparison of Performance of the Dynatherm Medical vitalHEAT™ Temperature Management System (vH2) and the Arizant Bair Hugger System
Study Type
Interventional

2. Study Status

Record Verification Date
September 2012
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
August 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of South Florida
Collaborators
Dynatherm Medical Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypothermia is a common and serious complication during anesthesia and surgery. Anesthetic-induced hypothermia results from the inhibition of thermoregulatory control and exposure to cold operating room environment. Various warming methods, such as warm blankets, forced-air warmers and circulating water mattresses, are currently used to prevent and treat mild perioperative hypothermia. All are cutaneous approaches that rely on heating the peripheral tissues in order to increase the thermal core temperature. Application of cutaneous warming system blankets/pads are limited by location/extent of operative site; for example, in certain procedures such as laparatomies, reconstructive plastic surgery or orthopedic surgery, only a limited amount of skin surface is available for warming application. The Dynatherm vitalHEAT technology takes advantage of the body's natural thermoregulatory system to channel thermal energy to the body's core non-invasively at a rapid rate. The vital heat (vH2) system is designed to treat hypothermia during the peri-operative period through a combination of localized heat and vacuum application to one hand & forearm; this application 1) opens the arteriovenous anastamoses located in the palm of the hand and 2) conductively warms the extremity thus effectively warming the blood flow to the body's core. The vital heat vH2 system is a portable and compact warming device which provides a non-invasive approach to warming patients during surgery. The primary objective of this study is to determine if the Dynatherm Medical vitalHEAT (vH2) Temperature Management System is as effective as the forced-air warming Bair Hugger™ (Arizant Healthcare, Eden Prairie, MN) for maintenance of intraoperative body temperature in patients undergoing abdominal surgery under general anesthesia. The critical endpoints to be evaluated in making this determination are 1) % of subjects with an average intraoperative esophageal temperature of ≥ 36º C and 2) % of subjects with an initial post anesthesia care unit sublingual temperature of ≥ 36º C. Secondary objectives include 1) comparison of the core body temperatures @ 60 minutes post anesthesia induction, 2) comparison of temperature trends during surgery and 3) comparison of the subjects' post anesthesia care unit temperature trends and hypothermic symptoms such as shivering.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypothermia
Keywords
intraoperative warming, anesthesia, hypothermia, body temperature

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
vH2 System Group
Arm Type
Experimental
Arm Description
The vital heat vH2 system consists of a Control Unit containing the heating system and the vacuum generation pump which connects via an umbilical containing the fluid and vacuum tubing to the Warming Sleeve. The Control Unit also contains the user interface and alarm management systems. The disposable Warming Sleeve consists of a manifold attached to the warming pads and a polyurethane pouch (Vacuum Sleeve) that are placed over the patient's hand and forearm and secured with tape. The Warming Sleeve manifold contains connectors for the fluid and vacuum tubing contained in the umbilical. The vital heat vH2 System will be used for patient warming during these surgical procedures. Monitoring of core temperature via esophageal probe will be done for the purpose of data collection.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
The Bair Hugger system is the current standard of care at Tampa General Hospital. It consists of a Temperature Management Unit that contains the heating element, the air circulating motor and the temperature control mechanisms. This unit connects via a hose to the operating room blankets. The Bair Hugger technology relies on heated air convection. Warm air is circulated evenly through the air space in the specially designed blanket, warming the skin surface as well as any insulating blankets placed over the Bair Hugger blanket. The Bair Hugger System is the site's current approach to patient warming during these surgical procedures. Monitoring of core temperature via esophageal probe will be done for the purpose of data collection.
Intervention Type
Device
Intervention Name(s)
Dynatherm Medical vitalHEAT Temperature Management System vH2
Other Intervention Name(s)
Part number VH-200
Intervention Description
The vH2 system consists of a Control Unit containing the heating system and the vacuum generation pump which connects via an umbilical containing the fluid and vacuum tubing to the Warming Sleeve. The Control Unit also contains the user interface and alarm management systems. The disposable Warming Sleeve consists of a manifold attached to the warming pads and a polyurethane pouch (Vacuum Sleeve) that are placed over the patient's hand and forearm and secured with tape. The Warming Sleeve manifold contains connectors for the fluid and vacuum tubing contained in the umbilical.
Intervention Type
Device
Intervention Name(s)
Bair Hugger™ (Arizant Healthcare, Eden Prairie, MN)
Other Intervention Name(s)
Model 522
Intervention Description
The Bair Hugger system is the current standard of care at Tampa General Hospital. It consists of a Temperature Management Unit that contains the heating element, the air circulating motor and the temperature control mechanisms. This unit connects via a hose to the operating room blankets. The Bair Hugger technology relies on heated air convection. Warm air is circulated evenly through the air space in the specially designed blanket, warming the skin surface as well as any insulating blankets placed over the Bair Hugger blanket.
Primary Outcome Measure Information:
Title
Percent of Patients With an Average Intraoperative Temperature Greater Than or Equal to 36 Celcius
Time Frame
Intraoperative Period
Title
Percent of Subjects With an Initial PACU Sublingual Temperature of ≥ 36º C.
Time Frame
Temp taken just prior to surgery
Title
Percentage of Patients With a Post Operative Sublingual Temperature Above 36 Degrees Celcius
Description
Percent of subjects with an initial post anesthesia care unit sublingual temperature of ≥ 36º C
Time Frame
Upon entry to the post anesthesia care unit
Secondary Outcome Measure Information:
Title
Comparison of the Core Body Temperatures at 60 Minutes Post Anesthesia Induction,as Assessed by Esophageal Probe.
Description
Average core body temperature measured with an esophageal probe at 60 minutes post-induction
Time Frame
60 minutes post anesthesia induction
Title
Average Intraoperative Esophageal Temperature
Description
Average esophageal temperature for the first 70 minutes of surgery following induction of anesthesia.
Time Frame
Intraoperative 0-70 minutes
Title
Median Post Anesthesia Care Unit Sublingual Temperature
Time Frame
Upon arrival to the post anesthesia care unit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients undergoing elective open abdominal surgical procedures with an expected duration of 2 to 4 hours and requiring general anesthesia American Society of Anesthesiologists(ASA) physical status I-III Patient age: > 18 years and <80 years Exclusion Criteria: Patient age: < 18 years and >80 years Patients with break in skin integrity on the extremity selected as the application site Patients with history of upper extremity peripheral vascular disease Patients with history of allergic skin conditions of the upper extremities Patients with history of bleeding disorders/coagulopathy Patient with history of malignant hyperthermia Patients who are pregnant Patient unwilling or unable to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enrico M Camporesi, M.D.
Organizational Affiliation
University of South Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tampa General Hospital
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17342966
Citation
Insler SR, Sessler DI. Perioperative thermoregulation and temperature monitoring. Anesthesiol Clin. 2006 Dec;24(4):823-37. doi: 10.1016/j.atc.2006.09.001.
Results Reference
background
PubMed Identifier
10691247
Citation
Sessler DI. Perioperative heat balance. Anesthesiology. 2000 Feb;92(2):578-96. doi: 10.1097/00000542-200002000-00042.
Results Reference
background
PubMed Identifier
15114200
Citation
Taguchi A, Ratnaraj J, Kabon B, Sharma N, Lenhardt R, Sessler DI, Kurz A. Effects of a circulating-water garment and forced-air warming on body heat content and core temperature. Anesthesiology. 2004 May;100(5):1058-64. doi: 10.1097/00000542-200405000-00005.
Results Reference
background
PubMed Identifier
8141463
Citation
Giesbrecht GG, Ducharme MB, McGuire JP. Comparison of forced-air patient warming systems for perioperative use. Anesthesiology. 1994 Mar;80(3):671-9. doi: 10.1097/00000542-199403000-00026.
Results Reference
background

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Intraoperative Warming Comparison of Devices

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