The Cardiac Effects of Prolonged Hypothermia After Cardiac Arrest
Primary Purpose
Cardiac Arrest, Hypothermia
Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Mild therapeutic hypothermia
Sponsored by
About this trial
This is an interventional treatment trial for Cardiac Arrest focused on measuring Cardiac arrest, Therapeutic Hypothermia, Cardioprotectiveness, Hemodynamics
Eligibility Criteria
Inclusion Criteria:
- Resuscitated after cardiac arrest outside hospital with suspected cardiac triggering cause (and stabile circulation for at least 20 minutes after return of spontaneous circulation,
- Glasgow coma score < 8 and
- Age ≥ 18 years and < 80 years.
Exclusion Criteria:
- Cardiac arrest of suspected non-cardiac triggering cause (e.g. trauma, aortic dissection, massive bleeding, hypoxia or accidental hypothermia),
- >60 minutes from cardiac arrest to ROSC,
- Time from cardiac arrest until start of cooling >4 hours,
- Terminal illness,
- Coagulopathy (medical anticoagulation treatment including thrombolysis is not a contraindication),
- Unwitnessed arrests with asystolia as presenting rhythm,
- Pregnancy,
- Persistent cardiogenic shock,
- Systolic blood pressure <80 mmHg despite vasoactive treatment and intra-aortic balloon pump
- CPC 3-4 before the cardiac arrest,
- Suspected/confirmed acute intra cerebral hemorrhage or stroke,
- Acute CABG or other operation in connection with performing CPR,
- Lack of consent from the relatives,
- Lack of consent from the GP and
- Lack of consent from the patient if he/she wakes up and is relevant.
Sites / Locations
- Department of Anesthesiology and Intensive Care Medicine, Aarhus University Hospital, Skejby
- Research Center of Emergency Medicine and Department of Anesthesiology and Intensive Care Medicine, Stavanger University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
24 hours mild therapeutic hypothermia
48 hours mild therapeutic hypothermia
Arm Description
The patient will be treated with mild therapeutic hypothermia for 24 hours after reaching the target temperature between 32-34°C.
The patient will be treated with mild therapeutic hypothermia for 48 hours after reaching the target temperature between 32-34°C.
Outcomes
Primary Outcome Measures
Area under the curve cTnT
Allocated sub study 1
Mitral annular systolic velocity
Allocated sub study 2
Duration of arrhythmias
Allocated sub study 3
Cumulative vasopressor index
Allocated sub study 3
Secondary Outcome Measures
Area under the curve NT-proBNP
Allocated sub study 1
Full Information
NCT ID
NCT02066753
First Posted
February 17, 2014
Last Updated
November 24, 2015
Sponsor
University of Aarhus
1. Study Identification
Unique Protocol Identification Number
NCT02066753
Brief Title
The Cardiac Effects of Prolonged Hypothermia After Cardiac Arrest
Official Title
The Cardiac Effects of Prolonged Hypothermia After Cardiac Arrest
Study Type
Interventional
2. Study Status
Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This PhD study is a sub study in a randomized clinical controlled multicenter trial named "TTH48" (ClinicalTrials.gov Identifier: NCT01689077).
The TTH48 trial examines prolonged mild therapeutic hypothermia ("MTH") at 32-34°C in 24 versus 48 hours with the primary outcome Cerebral Performance Category after 6 month in comatose out-of-hospital cardiac arrest patients.
THE OVERALL AIM OF THIS PhD STUDY IS TO INVESTIGATE THE CARDIAC FUNCTION AND THE HEMODYNAMICS BY BIOCHEMICAL CARDIAC MARKERS, ECHOCARDIOGRAPHY, BY ANALYZING THE USAGE OF INOTROPES/VASOPRESSORS AND BY ANALYZING ECG DATA FOR ARRHYTHMIAS IN THE 24 VERSUS 48 HOURS MTH GROUPS.
Detailed Description
The PhD-study contains 3 sub studies:
Study 1 estimates the extend of myocardial damage resulting from the primary arrest and from the reperfusion injuries: Area under the curve of cTnT and CK-MB as 12 repeated measurements and NT-proBNP as 4 measurements post arrest
-Hypothesis: There is a statistically significantly greater release of the cardiac biomarkers cTnT and NT-proBNP quantified by the area under the curve in the 24 versus the 48 hours group in the intervention period from 24 to 72 hours.
Study 2 investigates MTH´s influence on systolic and diastolic function by standard and Tissue Doppler (TDI) echocardiography after 24, 48 and 72 hours. The primary endpoint is mitral annular systolic velocity ("S´ max")
-Primary hypothesis: There is statistically significant improvement in S' max from the time T24 to T72 in the 48 versus the 24 hours group.
-Secondary hypothesis: There is statistically significantly better systolic function at T48 measured in terms of individual S' max-change in the 48 hours group (still hypothermic) versus the 24 hours group (reached normothermia).
Study 3 investigates MTH´s influence on the need for vasopressor or inotrope and the duration of arrhythmias during the first 72 hours post arrest.
Primary hypothesis: There is a statistically significantly increased tendency of arrhythmias in the 48 versus the 24 hours group measured in the period from T0 to T72.
Secondary hypothesis: There is a statistically significantly reduced need for inotropes in the 48 versus the 24 hours group measured by cumulative vasopressor index in the period from T0 to T72.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest, Hypothermia
Keywords
Cardiac arrest, Therapeutic Hypothermia, Cardioprotectiveness, Hemodynamics
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
24 hours mild therapeutic hypothermia
Arm Type
Active Comparator
Arm Description
The patient will be treated with mild therapeutic hypothermia for 24 hours after reaching the target temperature between 32-34°C.
Arm Title
48 hours mild therapeutic hypothermia
Arm Type
Experimental
Arm Description
The patient will be treated with mild therapeutic hypothermia for 48 hours after reaching the target temperature between 32-34°C.
Intervention Type
Procedure
Intervention Name(s)
Mild therapeutic hypothermia
Intervention Description
Mild therapeutic hypothermia with a target temperature between 32-34°C.
Primary Outcome Measure Information:
Title
Area under the curve cTnT
Description
Allocated sub study 1
Time Frame
In the intervention period from 24 to 72 hours
Title
Mitral annular systolic velocity
Description
Allocated sub study 2
Time Frame
After 24 hours, 48 hours and 72 hours
Title
Duration of arrhythmias
Description
Allocated sub study 3
Time Frame
From target temperature (32-34°C) has been reached until 72 hours after
Title
Cumulative vasopressor index
Description
Allocated sub study 3
Time Frame
From target temperature (32-34°C) has been reached until 72 hours after
Secondary Outcome Measure Information:
Title
Area under the curve NT-proBNP
Description
Allocated sub study 1
Time Frame
In the intervention period from 24 to 72 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Resuscitated after cardiac arrest outside hospital with suspected cardiac triggering cause (and stabile circulation for at least 20 minutes after return of spontaneous circulation,
Glasgow coma score < 8 and
Age ≥ 18 years and < 80 years.
Exclusion Criteria:
Cardiac arrest of suspected non-cardiac triggering cause (e.g. trauma, aortic dissection, massive bleeding, hypoxia or accidental hypothermia),
>60 minutes from cardiac arrest to ROSC,
Time from cardiac arrest until start of cooling >4 hours,
Terminal illness,
Coagulopathy (medical anticoagulation treatment including thrombolysis is not a contraindication),
Unwitnessed arrests with asystolia as presenting rhythm,
Pregnancy,
Persistent cardiogenic shock,
Systolic blood pressure <80 mmHg despite vasoactive treatment and intra-aortic balloon pump
CPC 3-4 before the cardiac arrest,
Suspected/confirmed acute intra cerebral hemorrhage or stroke,
Acute CABG or other operation in connection with performing CPR,
Lack of consent from the relatives,
Lack of consent from the GP and
Lack of consent from the patient if he/she wakes up and is relevant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders Grejs, MD
Organizational Affiliation
Research Center of Emergency Medicine and Department of Anesthesiology and Intensive Care Medicine, Aarhus University Hospital, Skejby, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Anesthesiology and Intensive Care Medicine, Aarhus University Hospital, Skejby
City
Aarhus N
State/Province
Central Denmark Region
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Research Center of Emergency Medicine and Department of Anesthesiology and Intensive Care Medicine, Stavanger University Hospital
City
Stavanger
ZIP/Postal Code
4068
Country
Norway
12. IPD Sharing Statement
Citations:
PubMed Identifier
33608045
Citation
Jensen TH, Juhl-Olsen P, Nielsen BRR, Heiberg J, Duez CHV, Jeppesen AN, Frederiksen CA, Kirkegaard H, Grejs AM. Echocardiographic parameters during prolonged targeted temperature Management in out-of-hospital Cardiac Arrest Survivors to predict neurological outcome - a post-hoc analysis of the TTH48 trial. Scand J Trauma Resusc Emerg Med. 2021 Feb 19;29(1):37. doi: 10.1186/s13049-021-00849-7.
Results Reference
derived
PubMed Identifier
28377297
Citation
Grejs AM, Nielsen BRR, Juhl-Olsen P, Gjedsted J, Sloth E, Heiberg J, Frederiksen CA, Jeppesen AN, Duez CHV, Hamre PD, Soreide E, Kirkegaard H. Effect of prolonged targeted temperature management on left ventricular myocardial function after out-of-hospital cardiac arrest - A randomised, controlled trial. Resuscitation. 2017 Jun;115:23-31. doi: 10.1016/j.resuscitation.2017.03.021. Epub 2017 Apr 2.
Results Reference
derived
Links:
URL
http://www.tth48.com
Description
Link to the parent trial: TTH48
Learn more about this trial
The Cardiac Effects of Prolonged Hypothermia After Cardiac Arrest
We'll reach out to this number within 24 hrs