Heated Humidification System Breathing Circuit for Maintenance of Body Temperature in Pediatric Patients (ANAPOD)
Primary Purpose
Temperature Change, Body
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Anapod™ Humi-Therm Heated Humidification System Breathing Circuit
Bair Hugger™ Warming Blanket
Sponsored by
About this trial
This is an interventional other trial for Temperature Change, Body focused on measuring Temperature management, Perioperative temperature management, Pediatric temperature management, Pediatric perioperative temperature management
Eligibility Criteria
Inclusion Criteria:
- Pediatric patients undergoing elective, scheduled dental procedures at Masonic Children's hospital requiring general anesthesia with endotracheal intubation, anticipated to last 1-6 hours or longer
Exclusion Criteria:
- Parent refusal of consent
- Patient refusal of assent (if applicable)
- Additional procedures (combined procedures) that involve other specialties besides dentists and other parts of the patient's body other than the oral cavity.
- History of diseases associated with temperature dysregulation (active hyperthyroidism, dysautonomia, osteogenesis imperfecta, history of malignant hyperthermia)
- Patients that will not be intubated for the procedure
Sites / Locations
- University of MinnesotaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Anapod™ Humi-Therm Heated Humidification System
Bair Hugger™ Warming Blanket
Arm Description
Patient warming will be provided via the Anapod™ Humi-Therm Heated Humidification System Breathing Circuit.
Patient warming will be provided via the Bair Hugger™ Warming Blanket.
Outcomes
Primary Outcome Measures
Rectal Temperature
Last measured core temperature at conclusion of the procedure (measured with rectal temperature probe) in patients assigned to the two warming systems.
Secondary Outcome Measures
Need for Hyperthermic or Hypothermic Rescue
Procedures for hyperthermic and hypothermic rescue can be found in the arm description section. Total number of rescue events will be compared between groups. A greater number of events indicates worse performance for that temperature control method.
Cumulative degree-minutes above and below 37C
Two temperature recording devices will be used: 3M SpotOn™ Forehead Temperature probe, (used routinely in the operating rooms and postoperative recovery areas) and a standard rectal thermistor probe. Cumulative minutes that patients spend above or below 37C will be compared between groups. A larger sum of degree-minutes above and below 37C indicates worse performance for that temperature control method.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03896867
Brief Title
Heated Humidification System Breathing Circuit for Maintenance of Body Temperature in Pediatric Patients
Acronym
ANAPOD
Official Title
Anapod™ Humi-Therm Heated Humidification System Breathing Circuit Versus Bair Hugger™ Warming Blanket for Intraoperative Maintenance of Body Temperature in Pediatric Patients Undergoing Dental Procedures: a Prospective Randomized Non-Inferiority Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 31, 2019 (Actual)
Primary Completion Date
October 1, 2024 (Anticipated)
Study Completion Date
October 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Our goal is to evaluate the efficacy of the Westmed system vs the Bair Hugger Blanket.
Detailed Description
Temperature management is an important aspect of perioperative care that falls under the purview of the anesthesiologist. Temperature is recognized as one of four primary vital signs and significant deviations from normal values may result in patient harm. General anesthesia disrupts the body's temperature homeostasis by inhibiting temperature regulation mechanisms such as vasoconstriction/-dilation, shivering and behavioral interventions (donning clothes or leaving an area with excessive heat, for example). Anesthetized patient have a tendency to become hypothermic, especially during long surgical procedures. This results from both the redistribution of cooler peripheral temperatures into the core (due to vasodilation) as well as actual temperature loss to a cold operating room environment (which is maintained at a lower temperature for the comfort of fully gowned surgeons and nurses). In addition, large surgical incisions predispose the patient to hypothermia through evaporation and convection.
Hypothermia is a recognized risk factor that predisposes the patient to an increased metabolic rate, increased oxygen demand, coagulopathies, impaired wound healing, impaired immune function and increased risk of infection. Therefore, maintenance of normal body temperature is an important goal of every general anesthetic - and is a well-accepted quality metric associated with patient care. Because of the greater surface area to volume relationship, children are thought to be a greater risk of intraoperative hypothermia.
The most widely used method of maintaining body temperature during surgery (and a routine at this institution) is by using a forced-air warming blanket (Bair Hugger warming blanket, 3M). Despite its widespread use, the forced-air warming blanket has its limitations. For example, during certain surgical procedures, the location of the surgical field precludes placement of the warming blanket. In addition, the warming blanket often cannot be placed immediately after the induction of anesthesia (when complex patient positioning is required) - leaving the patient exposed to hypothermic conditions for short (10-15min) or long (30-60min) periods of time. There is hence a need for alternative warming systems that could be implemented immediately following anesthetic induction.
Westmed, Inc. has developed an alternative system that utilizes a heated, humidified breathing circuit to regulate a patient's body temperature in the intraoperative setting. This system is active from the moment the trachea is intubated following anesthetic induction, i.e. there are no delays in instituting thermal management.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Temperature Change, Body
Keywords
Temperature management, Perioperative temperature management, Pediatric temperature management, Pediatric perioperative temperature management
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Masking Description
Group assignment will be blinded with the data set (Group A vs B) for review purposes - although it is important to note that true blinding of the providers (including on PI and Co PI) is impossible for this procedural study.
Allocation
Randomized
Enrollment
256 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Anapod™ Humi-Therm Heated Humidification System
Arm Type
Experimental
Arm Description
Patient warming will be provided via the Anapod™ Humi-Therm Heated Humidification System Breathing Circuit.
Arm Title
Bair Hugger™ Warming Blanket
Arm Type
Active Comparator
Arm Description
Patient warming will be provided via the Bair Hugger™ Warming Blanket.
Intervention Type
Device
Intervention Name(s)
Anapod™ Humi-Therm Heated Humidification System Breathing Circuit
Intervention Description
For the Anapod™ group, the BairHugger™ blanket will be connected, but the unit will not be turned on. The Anapod™ will be used with a starting circuit temperature set at the standard 45°C (note, this is temperature at the unit - NOT the temperature of the gas reaching the trachea). In the event that the patient's rectal temperature falls below 35.6C, the BairHugger™ warming system will be activated ("Hypothermic Rescue"). In the event that rectal temperature increases to a value of ≥37.5C, the Anapod system will be turned off - and the BairHugger turned on with the warming unit set to "ambient" (meaning cool operating room temperature will be blown over the patient ("Hyperthermic Rescue").
Intervention Type
Device
Intervention Name(s)
Bair Hugger™ Warming Blanket
Intervention Description
For the BairHugger™ group, the blanket will be used with a starting temperature set at HIGH. The BairHugger™ unit will be attached to the warming unit and started as soon as possible. In the event that the patient's rectal temperature falls below 35.6C, the Anapod™ warming system will be activated ("Rescue"). In the event that rectal temperature increases to a value of ≥37.5C, the BairHugger™ warming unit will be set to "ambient" (meaning cool operating room temperature will be blown over the patient ("Hyperthermic Rescue").
Primary Outcome Measure Information:
Title
Rectal Temperature
Description
Last measured core temperature at conclusion of the procedure (measured with rectal temperature probe) in patients assigned to the two warming systems.
Time Frame
study visit 1, at conclusion of dental procedure/anesthesia administration, approximately 1-6 hours
Secondary Outcome Measure Information:
Title
Need for Hyperthermic or Hypothermic Rescue
Description
Procedures for hyperthermic and hypothermic rescue can be found in the arm description section. Total number of rescue events will be compared between groups. A greater number of events indicates worse performance for that temperature control method.
Time Frame
study visit 1, measured continuously throughout dental procedure/anesthesia administration, approximately 1-6 hours
Title
Cumulative degree-minutes above and below 37C
Description
Two temperature recording devices will be used: 3M SpotOn™ Forehead Temperature probe, (used routinely in the operating rooms and postoperative recovery areas) and a standard rectal thermistor probe. Cumulative minutes that patients spend above or below 37C will be compared between groups. A larger sum of degree-minutes above and below 37C indicates worse performance for that temperature control method.
Time Frame
study visit 1, measured continuously throughout dental procedure/anesthesia administration, approximately 1-6 hours
10. Eligibility
Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
- Pediatric patients undergoing elective, scheduled dental procedures at Masonic Children's hospital requiring general anesthesia with endotracheal intubation, anticipated to last 1-6 hours or longer
Exclusion Criteria:
Parent refusal of consent
Patient refusal of assent (if applicable)
Additional procedures (combined procedures) that involve other specialties besides dentists and other parts of the patient's body other than the oral cavity.
History of diseases associated with temperature dysregulation (active hyperthyroidism, dysautonomia, osteogenesis imperfecta, history of malignant hyperthermia)
Patients that will not be intubated for the procedure
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Benjamin Kloesel, MD
Phone
612-625-6659
Email
bkloesel1@umn.edu
Facility Information:
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benjamin Kloesel
Phone
612-626-3284
Email
bkloesel@umn.edu
12. IPD Sharing Statement
Plan to Share IPD
No
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Heated Humidification System Breathing Circuit for Maintenance of Body Temperature in Pediatric Patients
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