Delayed Rewarming for Neuroprotection in Infants Following Cardiopulmonary Bypass Surgery
Primary Purpose
Post-Op Complication
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Strict normothermia
Delayed Rewarming
Sponsored by
About this trial
This is an interventional prevention trial for Post-Op Complication focused on measuring Therapeutic Hypothermia
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of congenital heart disease requiring congenital heart surgery on bypass
- Age less than 6 months at the time of surgery
- Intra-operative hypothermia less than or equal to 35°C
Exclusion Criteria:
- Concern for underlying coagulation disorder such as hemophilia
- Death in the operating room
- Inability to wean of cardiopulmonary bypass at conclusion of surgery
Sites / Locations
- Maine Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Strict Normothermia
Delayed Rewarming
Arm Description
Patients will be rewarmed to 36.5 degrees centigrade in the operating room and maintained here by conventional means in the PICU.
Patient will be rewarmed to 35.0 degrees centigrade in the operating room, then slowly rewarmed to normal physiologic temperature over 12 hours by using a servo-controlled cooling blanket. Normothermia will be maintained by the cooling blanket for an additional 12 hours.
Outcomes
Primary Outcome Measures
Infants With Elevated s100b and NSE
In a population of infants with congenital heart disease undergoing cardiopulmonary bypass surgery, does delayed rewarming administered during the 12 hours after surgery, compared to standard care, decrease brain injury as measured by levels of serum biomarkers of brain injury, s100b and neuron specific enolase during the four days after surgery?
Secondary Outcome Measures
Number of Participants With Adverse Events
In a population of infants with congenital heart disease undergoing cardiopulmonary bypass surgery, is there evidence for increased frequency of severe, moderate or other adverse events in the delayed rewarming group compared to the standard of care group?
Full Information
NCT ID
NCT03036072
First Posted
January 24, 2017
Last Updated
June 30, 2020
Sponsor
Alexa Craig
Collaborators
MaineHealth
1. Study Identification
Unique Protocol Identification Number
NCT03036072
Brief Title
Delayed Rewarming for Neuroprotection in Infants Following Cardiopulmonary Bypass Surgery
Official Title
Delayed Rewarming for Neuroprotection in Infants Following Cardiopulmonary Bypass Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
May 2016 (Actual)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
May 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Alexa Craig
Collaborators
MaineHealth
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is an unblinded, single center, randomized study of infants with congenital heart disease undergoing cardiopulmonary bypass surgery, randomized to either the delayed rewarming intervention or to the standard of care (strict normothermia).
Detailed Description
Control Group:
The congenital heart surgery will be performed according to usual practice with the degree of intra-operative hypothermia determined by the cardiothoracic surgeon based on the anticipated complexity of the case. Following completion of the surgical procedure, the infant will be rapidly rewarmed on CPB at a rate of 0.2 to 0.3°C per minute to a normothermic temperature of 36.5°C. Infants in this group will be given a single weight-based 15 mg/kg dose of intravenous Tylenol in the operating room (OR) by the anesthesiologist as the chest is being closed. The infant will be transported to the Pediatric Intensive Care Unit (PICU) for routine post-operative monitoring. If the infant develops a fever, ice packs will be applied to the axilla and groin per usual routine and removed once the fever has abated.
Experimental group:
Partial rewarming will occur on CPB to 35°C. During the last hour of surgery, the infant's temperature will be maintained at 35°C while the chest is closed by using a BairHugger and lowering the room temperature. Transfusions of packed red blood cells, fresh frozen plasma and cryoprecipitate will not be automatically warmed. Infants will be given a single 15 mg/kg dose of IV Tylenol in the OR. The infant will be transported to the PICU at 35°C and placed on the temperature-regulating blanket. The infant will be incrementally rewarmed with increases in temperature of 0.3°C every 2 hours for 6 hours, then 0.2°C every 2 hours for 6 hours to the goal temperature of 36.5°C. Once the infant is stable, EEG will be performed for 48 hours to screen for seizures. The PI will interpret the EEG every 6-8 hours. The infant will remain on the blanket at 36.5°C for another 12 hours. The blanket and esophageal temperature probe will then be removed a total of 24 hours after surgery was completed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-Op Complication
Keywords
Therapeutic Hypothermia
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Strict Normothermia
Arm Type
Active Comparator
Arm Description
Patients will be rewarmed to 36.5 degrees centigrade in the operating room and maintained here by conventional means in the PICU.
Arm Title
Delayed Rewarming
Arm Type
Experimental
Arm Description
Patient will be rewarmed to 35.0 degrees centigrade in the operating room, then slowly rewarmed to normal physiologic temperature over 12 hours by using a servo-controlled cooling blanket. Normothermia will be maintained by the cooling blanket for an additional 12 hours.
Intervention Type
Other
Intervention Name(s)
Strict normothermia
Intervention Type
Device
Intervention Name(s)
Delayed Rewarming
Intervention Description
Use of the servo-controlled cooling blanket for delayed rewarming to target temperature.
Primary Outcome Measure Information:
Title
Infants With Elevated s100b and NSE
Description
In a population of infants with congenital heart disease undergoing cardiopulmonary bypass surgery, does delayed rewarming administered during the 12 hours after surgery, compared to standard care, decrease brain injury as measured by levels of serum biomarkers of brain injury, s100b and neuron specific enolase during the four days after surgery?
Time Frame
4 days
Secondary Outcome Measure Information:
Title
Number of Participants With Adverse Events
Description
In a population of infants with congenital heart disease undergoing cardiopulmonary bypass surgery, is there evidence for increased frequency of severe, moderate or other adverse events in the delayed rewarming group compared to the standard of care group?
Time Frame
4 days
10. Eligibility
Sex
All
Maximum Age & Unit of Time
6 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of congenital heart disease requiring congenital heart surgery on bypass
Age less than 6 months at the time of surgery
Intra-operative hypothermia less than or equal to 35°C
Exclusion Criteria:
Concern for underlying coagulation disorder such as hemophilia
Death in the operating room
Inability to wean of cardiopulmonary bypass at conclusion of surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexa K Craig, MD, MSc
Organizational Affiliation
Assistant Professor of Pediatrics
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maine Medical Center
City
Portland
State/Province
Maine
ZIP/Postal Code
04102
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Delayed Rewarming for Neuroprotection in Infants Following Cardiopulmonary Bypass Surgery
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