Skip to main content
Clinical Trials/NCT02698319
NCT02698319
Completed
N/A

The Copenhagen Triage Algorithm

Herlev Hospital2 sites in 1 country50,000 target enrollmentApril 2015
ConditionsTriage

Overview

Phase
N/A
Intervention
Not specified
Conditions
Triage
Sponsor
Herlev Hospital
Enrollment
50000
Locations
2
Primary Endpoint
All cause mortality
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Crowding in the emergency department (ED) is a well documented problem putting patients at risk of adverse outcomes. To combat this, most ED's use some form of triage. In the last two decades systematic triage or process triage has become the norm in most countries but this approach is supported by limited evidence. Our aim is to develop a faster triage model of only a few vital parameters, based on a data from a large cohort of unselected ED patients and evaluate if such a model combined with a clinical assessment by the ED nurse is inferior to existing triage models in a prospective cluster-randomized trial

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
June 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rasmus Bo Hasselbalch

Medical student

Herlev Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients presenting acutely to the Acute ward/Emergency department in two hospitals in the Capital of Denmark

Exclusion Criteria

  • Patients presenting in Pediatric, Gynecological or Obstetric units

Outcomes

Primary Outcomes

All cause mortality

Time Frame: 30 days

Time frame starts at the beginning of the index admission, defined as first admission in the study period. Patients will be followed using central registers.

Secondary Outcomes

  • Number of patients with an admission to the intensive care unit(30 days)
  • Length of stay during admission(30 days)
  • Waiting time for treatment(8 hours)
  • Number of readmissions(30 and 90 days)
  • All cause mortality(90 days)

Study Sites (2)

Loading locations...

Similar Trials