- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01306734
Hypothermia and Circulatory Arrest During Surgery on the Ascending Aorta: A Comparison Between Two Cooling Methods
PURPOSE: To compare crash cooling versus gradient cooling methods for patients undergoing planned surgery on the ascending aorta in deep hypothermic circulatory arrest. To investigate the impact of hypothermia and circulatory arrest on the coagulation, stress-response, and cerebral outcome.
BACKGROUND: Cooling to 18 °C using extracorporeal circulation allows for circulatory arrest during surgery on the ascending aorta. Two different methods are used either lowering the temperature of the blood by 10 °C at a time, gradient cooling, or as cold as possible, crash cooling. The distribution of hypothermia is expected to be different for the two methods, the latter predominantly cooling the body core. The influence on the physiological response is expected to vary with the two methods. The surgical procedure and the cooling greatly elicit a stress response and the coagulation is profoundly influenced. There can be adverse effects on the neurological outcome due to the procedure. The two methods are considered equal, but have never been subjected to comparison. The surgery and circulatory changes can have a negative influence on the cerebral outcome .
METHODS: Twenty patients between 18 and 80 yrs randomized either to crash cooling or gradient cooling, ten patients in each group.. Patients with severe comorbidities or known coagulopathy are excluded. Anesthesia and operation as performed routinely in the department. The primary endpoint is duration of cooling, secondary endpoints include coagulation parameters (thromboelastography, clot stability), stress response parameters (adhesion molecule expression on endothelial cells, oxidative stress analysis, inflammatory markers), neuropsychological tests, MRI of the cerebrum, markers of cerebral ischemia, and ultrasound imaging of the great vessels for detection of air bubbles. Baseline values are obtained for all parameters.
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Hans Kirkegaard, MD, Ph.D.
- Phone Number: +4589498852
- Email: hans.kirkegaard@dadlnet.dk
Study Contact Backup
- Name: Kristian K Andersen, MD
- Phone Number: +4521680494
- Email: kristian.kjaer.andersen@ki.au.dk
Study Locations
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Aarhus N
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Aarhus, Aarhus N, Denmark, 8200
- Recruiting
- Department of Anesthesia and Intensive Care, Aarhus University Hospital, Skejby
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Contact:
- Kristian K Andersen, MD
- Email: kristianka@gmail.com
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Principal Investigator:
- Hans Kirkegaard, MD, Ph.D.
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients scheduled for surgery on the ascending aorta
- Need for deep hypothermic circulatory arrest during the procedure
Exclusion Criteria:
- Known coagulopathy
- Ejection fraction less than 30 %
- Severe psychiatric or neurological disease
- Severe liver disease
- Severely reduced lung function
- Glomerular filtration rate less than 15 ml/min/1.73 m2
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Gradient cooling group
Study group receiving gradient cooling during the procedure using extracorporeal circulation (ECC).
The procedure is used routinely in the department and is not an experimental procedure.
A maximum of 10 degrees celsius is allowed between the measured nasopharyngeal body temperature and the heater-cooler unit of the ECC-machine, when cooling or rewarming.
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Crash cooling group
Study group receiving rapid cooling using extracorporeal circulation.
The protocol for rapid cooling is using routinely in the department and is not an experimental procedure.
When cooling, the investigators aim for maximal difference in temperature between the heater-cooler unit of the ECC-machine.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Duration of cooling
Time Frame: intraoperatively
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intraoperatively
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
MRI of cerebrum
Time Frame: Baseline prior to surgery and 4 to 5 days postoperatively
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Standard perfusion-weighed Magnetic Resonance imaging of the cerebrum.
The same investigator describes all images.
No use of contrast agents.
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Baseline prior to surgery and 4 to 5 days postoperatively
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Markers of neurological injury
Time Frame: baseline, postoperative
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s-100b, Neuron specific enolase
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baseline, postoperative
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neurological exam
Time Frame: baseline, postoperative, after 4 months
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baseline, postoperative, after 4 months
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cognitive test
Time Frame: baseline, postoperative, after 4 months
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baseline, postoperative, after 4 months
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markers of elevated inflammatory response
Time Frame: perioperatively
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perioperatively
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Markers of oxidative stress
Time Frame: perioperatively
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perioperatively
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Coagulation parameters
Time Frame: perioperatively
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perioperatively
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HYPO-SKS-2011
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