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NCT Number: NCT00650260

Intraoperative Warming Comparison of Devices

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tampa General Hospital

Tampa, Florida, 33606, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Dynatherm Medical vitalHEAT Temperature Management System vH2

Device

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.

Other names: Part number VH-200

Bair Hugger™ (Arizant Healthcare, Eden Prairie, MN)

Device

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.

Other names: Model 522

Primary outcomes

  1. Percent of Patients With an Average Intraoperative Temperature Greater Than or Equal to 36 Celcius

    Time frame: Intraoperative Period

  2. Percent of Subjects With an Initial PACU Sublingual Temperature of ≥ 36º C.

    Time frame: Temp taken just prior to surgery

  3. Percentage of Patients With a Post Operative Sublingual Temperature Above 36 Degrees Celcius

    Time frame: Upon entry to the post anesthesia care unit

    Percent of subjects with an initial post anesthesia care unit sublingual temperature of ≥ 36º C

Secondary outcomes

  1. Comparison of the Core Body Temperatures at 60 Minutes Post Anesthesia Induction,as Assessed by Esophageal Probe.

    Time frame: 60 minutes post anesthesia induction

    Average core body temperature measured with an esophageal probe at 60 minutes post-induction

  2. Average Intraoperative Esophageal Temperature

    Time frame: Intraoperative 0-70 minutes

    Average esophageal temperature for the first 70 minutes of surgery following induction of anesthesia.

  3. Median Post Anesthesia Care Unit Sublingual Temperature

    Time frame: Upon arrival to the post anesthesia care unit

Sponsors and collaborators

Lead sponsor

University of South Florida

Other

Collaborators

  • Dynatherm Medical Inc.

Registry information

Official study title

Intraoperative Warming : Comparison of Performance of the Dynatherm Medical vitalHEAT™ Temperature Management System (vH2) and the Arizant Bair Hugger System

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Apr 1, 2008
Registry last updated
Oct 29, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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