Epidemiology and Cost-effectiveness of Out-Of-Hospital Cardiac Arrest in Finland (FINNRESUSCI)

This study has been completed.
Sponsor:
Collaborator:
Helsinki University Central Hospital
Information provided by (Responsible Party):
jouni kurola, Kuopio University Hospital
ClinicalTrials.gov Identifier:
NCT01295424
First received: February 9, 2011
Last updated: January 30, 2015
Last verified: January 2015

February 9, 2011
January 30, 2015
March 2010
October 2014   (final data collection date for primary outcome measure)
Alive at hospital discharge (time frame: Hospital discharge day) [ Time Frame: 12 hours ] [ Designated as safety issue: No ]
alive at hospital discharge
Alive at hospital discharge [ Time Frame: 12 hours ] [ Designated as safety issue: No ]
alive at hospital discharge
Complete list of historical versions of study NCT01295424 on ClinicalTrials.gov Archive Site
CPC (time frame: 1 year after cardiac arrest) [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Neurologic outcome (Cerebral Performance Category) at one year after out of hospital cardiac arrest.
CPC [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Neurologic outcome (Cerebral Performance Category) at one year after out of hospital cardiac arrest.
Not Provided
Not Provided
 
Epidemiology and Cost-effectiveness of Out-Of-Hospital Cardiac Arrest in Finland
FinnResusci: Epidemiology and Cost-effectiveness of Out-Of-Hospital Cardiac Arrest in Finland
Observational study of all out-of-hospital cardiac arrest during 6 months in regional areas of Helsinki University Hospital and Kuopio University Hospital from activation of EMS system until follow up to 6 months of survival.Simultaneous observation of out-of-hospital cardiac arrest primary survivors admitted to all Finnish ICUs.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Retention:   Samples Without DNA
Description:
Blood
Non-Probability Sample
Out-of-hospital cardiac arrest patients
Cardiac Arrest
Other: No intervention
Observational study, no interventions
Single group study
Intervention: Other: No intervention
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
2600
October 2014
October 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Out-of-hospital cardiac arrest patients

Exclusion Criteria:

Both
Child, Adult, Senior
No
Contact information is only displayed when the study is recruiting subjects
Finland
 
NCT01295424
KUH 5070212
No
Not Provided
Not Provided
jouni kurola, Kuopio University Hospital
Kuopio University Hospital
Helsinki University Central Hospital
Study Director: Tom Silfvast, MD, PhD Helsinki University Central Hospital
Kuopio University Hospital
January 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP