NL-OMON36855
Completed
Not Applicable
Cognitive impairment following cardiac arrest and Target Temperature Management (A sub-study of the TTM Trial) - Cognitive impairment following cardiac arrest
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- cognitive disorders
- Sponsor
- Academisch Medisch Centrum
- Enrollment
- 85
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. TTM study patients who are alive at six\-month follow\-up and give consent to the cognitive sub\-study
- •2\. Informants (usually a relative or close friend/caregiver) of the patient above (1\) who give consent to the cognitive sub\-study
- •3\. STEMI patients at the given centre, the sex\-matched patient who best fits in age to the TMM patient above (1\) with a similar date of infarct who gives consent to the cognitive sub\-study
- •4\. Informants (usually a relative or close friend/caregiver) of 3 above who give consent to participate.
Exclusion Criteria
- •The same exclusion criteria as for the main TTM study with the addition that control patients should not have a history of cardiac arrest.
- •Exclusion criteria TTM study: Conscious patients, pregnancy, out\-of\-hospital cardiac arrest of presumed non\-cardiac cause, cardiac arrest after arrival in hospital, known bleeding diathesis, suspected or confirmed acute intracranial bleeding, suspected or confirmed acute stroke, temperature on admission \<30°C, unwitnessed asystole, persistent cardiogenic shock, known limitations in therapy, known disease making 180 day survival unlikely, known pre\-arrest cerebral performance category 3 or 4, \>240 minutes from ROSC to randomisation, no informed consent.
Outcomes
Primary Outcomes
Not specified
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