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Clinical Trials/NCT00998140
NCT00998140
Unknown
Not Applicable

Optimizing Resuscitation After Cardiac Arrest in the Community: Increasing the Probability of Survival While Reducing Costs

Shaare Zedek Medical Center1 site in 1 country1,600 target enrollmentMarch 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiopulmonary Arrest Outcome
Sponsor
Shaare Zedek Medical Center
Enrollment
1600
Locations
1
Last Updated
5 years ago

Overview

Brief Summary

Resuscitative efforts have been shown to be unsuccessful in most cases of out-of-hospital cardiac arrest (OHCA), and survivors who do recover cardiac function often sustain severe hypoxic brain damage. Time to efficacious care is a primary determinant of disability-free survival. In the Jerusalem district, only 9% of OHCA patients present with ventricular tachycardia/ventricular fibrillation (VT/VF) as the primary rhythm, whereas 77% present with asystole; this seems primarily to be the result of long collapse-to-arrival times. Nevertheless, overly zealous resuscitation is undertaken in a high proportion of arrests with a futile prognosis, leading to excessive costs.

Study hypotheses:

  1. Subpopulations for whom intervention is futile/counter-productive are identifiable
  2. Substantial waste of resources can be avoided
  3. Optimization of emergency medical services (EMS) reorganization without adding resources is an achievable goal
Registry
clinicaltrials.gov
Start Date
March 2009
End Date
October 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr Sharon Einav

Dr.

Shaare Zedek Medical Center

Eligibility Criteria

Inclusion Criteria

  • All victims of non-traumatic out-of hospital cardiopulmonary arrest (defined as the absence of either spontaneous respiration or palpable pulse or both) within the Jerusalem district.

Exclusion Criteria

  • Patients with do-not-resuscitate orders or an advance directive to that effect.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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