Skip to main content
Clinical Trials/NL-OMON36855
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

Academisch Medisch Centrum0 sites85 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

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

Similar Trials