Intraoperative Warming During Major Surgical Procedures Using the Esophageal Temperature Management System
Primary Purpose
Hypothermia Following Anesthesia, Hypothermia, Surgery
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EnsoETM
Surface Warming
Sponsored by
About this trial
This is an interventional prevention trial for Hypothermia Following Anesthesia focused on measuring intraoperative hypothermia, inadvertent hypothermia, perioperative hypothermia
Eligibility Criteria
Inclusion Criteria:
- Provision of signed and dated informed consent form
- Male or female, ages 18 years and older
- Scheduled for major surgical procedures requiring general anesthesia and with no known contraindication to having an orogastric tube placed for the duration of the surgery
- The time in the OR is expected to last at least 180 minutes
Exclusion Criteria:
- Esophageal strictures (risk of perforation)
- Patients with known esophageal deformity or evidence of esophageal trauma (for example history of esophagectomy, previous swallowing disorders, achalasia, etc.)
- Known ingestion of acidic or caustic poisons within the prior 24 hours.
- Patients with <40 kg of body mass
- Coagulopathy
- Severe facial trauma
- Surgical procedures lasting less than 3 hours
Sites / Locations
- Thomas Jefferson University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
EnsoETM
Standard of Care
Arm Description
Participants receive esophageal warming. Original study design anticipated esophageal warming in addition to standard of care surface warming from the time they enter the OR until released to the PACU. After 7 patients, protocol was adjusted to specify only esophageal warming unless addition of surface warming was warranted.
Participants receive standard of care surface warming from the time they enter the OR until released to the PACU.
Outcomes
Primary Outcome Measures
Inadvertent Hypothermia Prevention
Number of degree-hours spent below 37 °C intraoperatively until recovery in the PACU and return to 37°C body temperature.
Secondary Outcome Measures
Time From Intubation Until Extubation
Time from intubation until extubation
Full Information
NCT ID
NCT03790683
First Posted
December 27, 2018
Last Updated
January 30, 2023
Sponsor
Advanced Cooling Therapy, Inc., d/b/a Attune Medical
Collaborators
Thomas Jefferson University
1. Study Identification
Unique Protocol Identification Number
NCT03790683
Brief Title
Intraoperative Warming During Major Surgical Procedures Using the Esophageal Temperature Management System
Official Title
Intraoperative Warming During Major Surgical Procedures Using the Esophageal Temperature Management System
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Terminated
Why Stopped
Sponsor funding limitations
Study Start Date
February 11, 2019 (Actual)
Primary Completion Date
August 1, 2021 (Actual)
Study Completion Date
December 1, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Advanced Cooling Therapy, Inc., d/b/a Attune Medical
Collaborators
Thomas Jefferson University
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
Yes
5. Study Description
Brief Summary
The aim of this study is to assess the effectiveness of EnsoETM as a supplemental warming device compared to the standard of care warming practice in patients having major surgery.
Detailed Description
Maintaining patient's body temperature is of major importance in patients undergoing surgical procedures and existing methods to warm patients to maintain perioperative normothermia have limitations. This results in as many as half of patients undergoing surgery developing inadvertent hypothermia during and/or after their procedure. The EnsoETM is an Esophageal Temperature Management (ETM) device consisting of a multi-chambered silicone tube connected to a heat exchanger and placed in the esophagus, providing highly efficient heat transfer to a patient. The EnsoETM potentially improves the ability to control patient temperature by eliminating the disadvantages of existing methods while maintaining the functionality of the orogastric tube that it replaces.
The primary objective of this study is to measure the number of degree-hours spent below 37°C intraoperatively and until recovery in the PACU. This measure will be compared between patients having standard management of body temperature to patients having the EnsoETM placed as an additional warming device.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypothermia Following Anesthesia, Hypothermia, Surgery
Keywords
intraoperative hypothermia, inadvertent hypothermia, perioperative hypothermia
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective, randomized interventional study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EnsoETM
Arm Type
Experimental
Arm Description
Participants receive esophageal warming. Original study design anticipated esophageal warming in addition to standard of care surface warming from the time they enter the OR until released to the PACU. After 7 patients, protocol was adjusted to specify only esophageal warming unless addition of surface warming was warranted.
Arm Title
Standard of Care
Arm Type
Active Comparator
Arm Description
Participants receive standard of care surface warming from the time they enter the OR until released to the PACU.
Intervention Type
Device
Intervention Name(s)
EnsoETM
Other Intervention Name(s)
ECD02, Esophageal Cooling Device
Intervention Description
Patients having major surgery will have the EnsoETM device placed after induction of general anesthesia. Addition of standard of care surface warming was specified as optional after first 7 patients.
Intervention Type
Device
Intervention Name(s)
Surface Warming
Other Intervention Name(s)
Bair Hugger, forced air blanket
Intervention Description
Forced air warming device will be placed on the patient according to standard practice.
Primary Outcome Measure Information:
Title
Inadvertent Hypothermia Prevention
Description
Number of degree-hours spent below 37 °C intraoperatively until recovery in the PACU and return to 37°C body temperature.
Time Frame
Time from intubation until extubation, approximately 3-12 hours
Secondary Outcome Measure Information:
Title
Time From Intubation Until Extubation
Description
Time from intubation until extubation
Time Frame
perioperative, approximately 3-12 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Provision of signed and dated informed consent form
Male or female, ages 18 years and older
Scheduled for major surgical procedures requiring general anesthesia and with no known contraindication to having an orogastric tube placed for the duration of the surgery
The time in the OR is expected to last at least 180 minutes
Exclusion Criteria:
Esophageal strictures (risk of perforation)
Patients with known esophageal deformity or evidence of esophageal trauma (for example history of esophagectomy, previous swallowing disorders, achalasia, etc.)
Known ingestion of acidic or caustic poisons within the prior 24 hours.
Patients with <40 kg of body mass
Coagulopathy
Severe facial trauma
Surgical procedures lasting less than 3 hours
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Coleen Vernick, DO
Organizational Affiliation
Thomas Jefferson University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Intraoperative Warming During Major Surgical Procedures Using the Esophageal Temperature Management System
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