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Comparison of Active and Passive Perioperative Warming Techniques in Reducing Intraoperative Blood Loss

Primary Purpose

Hypothermia, Blood Loss,, Blood Coagulation Disorders

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Bair Hugger forced air warming system
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypothermia focused on measuring perioperative hypothermia, Tympanic temperature, Blood loss, Blood Coagulation Disorders, Major surgery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients≥18 years old
  • Preoperative core temperature between 36.0 and 37.5°C
  • American Society of Anaesthesiologists(ASA) Physical Status Classification System I-III
  • No transdermal meds on the target site
  • Elective major surgeries included but not limited:

    • Hip replacement
    • Thoracic surgery (lobectomy and esophagectomy) or abdominal surgery

Exclusion Criteria:

  • Less than 18 years old
  • Uncontrolled insulin-dependent diabetes mellitus (preoperative glucose >250 mg/dL)
  • A preoperative temperature above 37.5°C or less than 36°C
  • Hyperthyroidism and hypothyroidism
  • Raynaud disease
  • History of infection and fever within 4 weeks before surgery
  • Use of steroid or immunosuppressant within 4 weeks before surgery
  • History of bleeding disorders
  • Clinically significant laboratory abnormalities
  • Hgb ≤ 10.0 g/L
  • Platelets ≤ 100,000 / mL
  • WBC(white blood cell ) <3000/dL
  • Fibrinogen<200 mg/dL
  • Thromboplastin time>40s
  • Prothrombin time
  • international normalized ratio(INR)<70%

Sites / Locations

  • Peking Union Medical College Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Bair hugger forced air warming therapy

conventional warming care

Arm Description

Use of Bair Hugger forced-air warming system perioperatively to keep patient normothermia

conventional warming care

Outcomes

Primary Outcome Measures

Core Temperature and blood loss
Monitor the changes of core temperature for whole perioperative period and the amount of blood loss were recorded

Secondary Outcome Measures

Length of Stay in PACU
Length of Stay in Hospital
Length of Stay in ICU
Surgical Site Infection(SSI)
coagulation function
take blood sample to detect the coagulation function,including Prothrombin time,Active Partial Thromboplastin Time,International normalized Ratio,Thromboelastography,Hemoglobin,ect.

Full Information

First Posted
August 8, 2014
Last Updated
August 15, 2014
Sponsor
Peking Union Medical College Hospital
Collaborators
3M
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1. Study Identification

Unique Protocol Identification Number
NCT02214524
Brief Title
Comparison of Active and Passive Perioperative Warming Techniques in Reducing Intraoperative Blood Loss
Official Title
Comparison of Active Warming System and Conventional Passive Warming Care in Reducing Intraoperative Blood Loss for Patients Undergoing Major Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Unknown status
Study Start Date
August 2014 (undefined)
Primary Completion Date
November 2014 (Anticipated)
Study Completion Date
January 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking Union Medical College Hospital
Collaborators
3M

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomized, open label, parallel two arm, clinical study, which compare the Bair Hugger forced-air warming blanket and the conventional warming care practice in China on patients undergoing major surgery to determine the impact of maintaining normothermia on intraoperative blood loss, requirement for transfusion of packed red blood cells and the changes of coagulation function.
Detailed Description
Each Investigator reviews the most current Instructions for Use for Bair Hugger Forced air Warming System to assess the contraindications, warnings, and precaution sections with respect to risks and benefits for treating potential patients. 60 patients will be enrolled preliminary in this clinical trial. Equal size of 30 patients were allocated randomly into interventional or control group. Randomization will be performed after the patient has met all eligibility criteria, including the general inclusion or exclusion and the patient or legally authorized representative has signed an informed consent form prior to any study related procedure. Prior to induction, patients in the interventional group were provided 15 to 30 minutes forced air warming using the Bair Hugger warming unit, either in the pre-anesthesia area or OR,which may add to the total heat content of the body helping to reduce the effects of redistribution temperature drop for procedures using a temperature management strategy. The Bair Hugger warming unit is placed on its highest temperature setting and will be adjusted by the investigator depending on temperature monitoring. Temperature will be measured in both groups by either Spot-On sensor and tympanic membrane thermometer. Statistical analysis will be performed after the data of 30 cases (both groups) were available and the sample size will be re-estimated based on preliminary data analysis. Continuous variables will be summarized with mean, median, standard deviation, minimum and maximum, as applicable. Categorical variables will be summarized with frequency and percentage. Student t test will be used to compare means for continuous variables. A Chi square test or a Fisher's exact test will be used to compare proportions for categorical variables. Multiple regression will be performed to assess the risk ratios of patients developing hypothermia and will be expressed as an risk ratio along with a 95% confidence interval.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypothermia, Blood Loss,, Blood Coagulation Disorders
Keywords
perioperative hypothermia, Tympanic temperature, Blood loss, Blood Coagulation Disorders, Major surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bair hugger forced air warming therapy
Arm Type
Experimental
Arm Description
Use of Bair Hugger forced-air warming system perioperatively to keep patient normothermia
Arm Title
conventional warming care
Arm Type
No Intervention
Arm Description
conventional warming care
Intervention Type
Device
Intervention Name(s)
Bair Hugger forced air warming system
Other Intervention Name(s)
Bair Hugger 775, 70-2007-6800, Bair Hugger Blanket Model 635 and 300
Intervention Description
Bair Hugger Model 775 temperature management unit-offers two airflow settings, hose-end temperature sensing, and precise temperature delivery
Primary Outcome Measure Information:
Title
Core Temperature and blood loss
Description
Monitor the changes of core temperature for whole perioperative period and the amount of blood loss were recorded
Time Frame
intraoperative
Secondary Outcome Measure Information:
Title
Length of Stay in PACU
Time Frame
90 days after Hip replacement surgery and 30 days after other surgerys
Title
Length of Stay in Hospital
Time Frame
90 days after Hip replacement surgery and 30 days after other surgerys
Title
Length of Stay in ICU
Time Frame
90 days after Hip replacement surgery and 30 days after other surgerys
Title
Surgical Site Infection(SSI)
Time Frame
90 days after Hip replacement surgery and 30 days after other surgerys
Title
coagulation function
Description
take blood sample to detect the coagulation function,including Prothrombin time,Active Partial Thromboplastin Time,International normalized Ratio,Thromboelastography,Hemoglobin,ect.
Time Frame
perioperative period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients≥18 years old Preoperative core temperature between 36.0 and 37.5°C American Society of Anaesthesiologists(ASA) Physical Status Classification System I-III No transdermal meds on the target site Elective major surgeries included but not limited: Hip replacement Thoracic surgery (lobectomy and esophagectomy) or abdominal surgery Exclusion Criteria: Less than 18 years old Uncontrolled insulin-dependent diabetes mellitus (preoperative glucose >250 mg/dL) A preoperative temperature above 37.5°C or less than 36°C Hyperthyroidism and hypothyroidism Raynaud disease History of infection and fever within 4 weeks before surgery Use of steroid or immunosuppressant within 4 weeks before surgery History of bleeding disorders Clinically significant laboratory abnormalities Hgb ≤ 10.0 g/L Platelets ≤ 100,000 / mL WBC(white blood cell ) <3000/dL Fibrinogen<200 mg/dL Thromboplastin time>40s Prothrombin time international normalized ratio(INR)<70%
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hao Liang
Phone
+86 13391994260
Email
805582814@qq.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ruiyue Song
Phone
+86 13261916376
Email
575514878@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yugung Huang Huang, doctoral
Organizational Affiliation
Peking Union Medical College Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking Union Medical College Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100000
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jie YI, doctoral
Phone
+86 10 69152025
Email
neyil@pumch.cn
First Name & Middle Initial & Last Name & Degree
Yuguang Huang, doctoral
First Name & Middle Initial & Last Name & Degree
Jie Yi, doctoral

12. IPD Sharing Statement

Citations:
PubMed Identifier
30193571
Citation
Yi J, Liang H, Song R, Xia H, Huang Y. Maintaining intraoperative normothermia reduces blood loss in patients undergoing major operations: a pilot randomized controlled clinical trial. BMC Anesthesiol. 2018 Sep 8;18(1):126. doi: 10.1186/s12871-018-0582-9.
Results Reference
derived

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Comparison of Active and Passive Perioperative Warming Techniques in Reducing Intraoperative Blood Loss

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