We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov
ClinicalTrials.gov Menu

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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01295424
Recruitment Status : Completed
First Posted : February 14, 2011
Last Update Posted : February 2, 2015
Sponsor:
Collaborator:
Information provided by (Responsible Party):

Study Description
Brief Summary:
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.

Condition or disease Intervention/treatment
Cardiac Arrest Other: No intervention

Study Design

Study Type : Observational
Actual Enrollment : 2600 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: FinnResusci: Epidemiology and Cost-effectiveness of Out-Of-Hospital Cardiac Arrest in Finland
Study Start Date : March 2010
Primary Completion Date : October 2014
Study Completion Date : October 2014

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Groups and Cohorts

Group/Cohort Intervention/treatment
Single group study Other: No intervention
Observational study, no interventions


Outcome Measures

Primary Outcome Measures :
  1. Alive at hospital discharge (time frame: Hospital discharge day) [ Time Frame: 12 hours ]
    alive at hospital discharge


Secondary Outcome Measures :
  1. CPC (time frame: 1 year after cardiac arrest) [ Time Frame: 1 year ]
    Neurologic outcome (Cerebral Performance Category) at one year after out of hospital cardiac arrest.


Biospecimen Retention:   Samples Without DNA
Blood

Eligibility Criteria

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Out-of-hospital cardiac arrest patients
Criteria

Inclusion Criteria:

  • Out-of-hospital cardiac arrest patients

Exclusion Criteria:

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01295424


Locations
Finland
Kuopio University Hospital
Kuopio, Finland, 70211
Sponsors and Collaborators
Kuopio University Hospital
Helsinki University Central Hospital
Investigators
Study Director: Tom Silfvast, MD, PhD Helsinki University Central Hospital
More Information

Responsible Party: jouni kurola, Chief Physician, Kuopio University Hospital
ClinicalTrials.gov Identifier: NCT01295424     History of Changes
Other Study ID Numbers: KUH 5070212
First Posted: February 14, 2011    Key Record Dates
Last Update Posted: February 2, 2015
Last Verified: January 2015

Keywords provided by jouni kurola, Kuopio University Hospital:
Cardiac Arrest
Intensive Care Unit
Emergency Medical Service

Additional relevant MeSH terms:
Heart Arrest
Out-of-Hospital Cardiac Arrest
Heart Diseases
Cardiovascular Diseases