Quality of Cardiopulmonary Resuscitation Pre- and Intra Hospital
1 other identifier
observational
300
0 countries
N/A
Brief Summary
The survival after intrahospital cardiac arrest has been reported to 15%. In Norway this varies between 16 and 23%.). Many factors are associated with survival after cardiac arrest, both intra- and prehospital. Recent studies have not included information about individual patient factors and the outcome after cardiopulmonary resuscitation (CPR). In the current hospital, we are able to record patient specific information related to a cardiac arrest/CPR situation, and thereby be able to assess patient-related factors associated with both detection, treatment and outcome of CPR.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2026
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 5, 2020
CompletedFirst Posted
Study publicly available on registry
March 4, 2020
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2028
August 5, 2025
August 1, 2025
2 years
January 5, 2020
August 3, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Mortality
Patient dead or alive
up to 30 days
Eligibility Criteria
All patients with cardiac arrest, treated with cardio-pumonary resusciation and the use of a defirbillator with USB memory stick installed (all 71 in the current hospital)
You may qualify if:
- cardiac arrest (all reasons)
- a defibrillator has been used
- over 18 years
- cardiopulmonary resuscitation has been conducted
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Target Duration
- 6 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
January 5, 2020
First Posted
March 4, 2020
Study Start
January 1, 2026
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
December 31, 2028
Last Updated
August 5, 2025
Record last verified: 2025-08