Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
42 participants
OBSERVATIONAL
2015-10-31
2016-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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cardiac arrest patients
Patients who has suffered a cardiac arrest
cardiac arrest
Interventions
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cardiac arrest
Eligibility Criteria
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Inclusion Criteria
* Return of spontaneous circulation (ROSC)
* Glasgow Coma Score \< 8
* Age \> 18 years and \< 80 years
Exclusion Criteria
* Time interval \> 4 hours from cardiac arrest to initiation of targeted temperature management
* Terminal illness
* Coagulation disorder
* Unwitnessed asystolia
* Cerebral performance category 3-4 before the cardiac arrest
* Severe persistent cardiogenic shock
* Pregnancy
* Persistent cardiogenic shock (systolic blood pressure \< 80 despite inotropic treatment)
* New apoplexy or intracerebral hemorrhage
* Lack of consent from the relatives
* Lack of consent from the general practitioner
* Lack of consent from the patient if he/she wakes up and is relevant
18 Years
80 Years
ALL
Yes
Sponsors
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University of Aarhus
OTHER
Responsible Party
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Locations
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Dept of Anesthesiology and Intensive Care and Dept of Clinical Biochemistry, Aarhus University Hospital
Aarhus, Aarhus N, Denmark
Countries
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Other Identifiers
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AU170878
Identifier Type: -
Identifier Source: org_study_id
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