The Copenhagen Triage Algorithm (CTA)

August 15, 2016 updated by: Rasmus Bo Hasselbalch, Herlev Hospital
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

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

50000

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Region Hovedstaden
      • Herlev, Region Hovedstaden, Denmark, 2730
        • Herlev Hospital
      • København NV, Region Hovedstaden, Denmark, 2400
        • Bispebjerg Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Conventional Triage
Conventional triage using Danish Emergency Process Triage (DEPT).
Experimental: Copenhagen Triage Algorithm
The Copenhagen Triage Algorithm is used as triage form in the ED. The Copenhagen Triage Algorithm consists of a few vital parameters and a clinical assessment from the ED nurse.
The Copenhagen Triage Algorithm is a new triage method for faster triage in the ED

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
30 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
All cause mortality
Time Frame: 90 days
90 days
Number of patients with an admission to the intensive care unit
Time Frame: 30 days
30 days
Length of stay during admission
Time Frame: 30 days
30 days
Waiting time for treatment
Time Frame: 8 hours
Waiting time from first presenting at ED to first treatment startet
8 hours
Number of readmissions
Time Frame: 30 and 90 days
Patients will be followed using central registers. All new admissions within 91 days of the same patient is defined as readmissions.
30 and 90 days
All cause mortality
Time Frame: 48 hours
48 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Kasper Iversen, MD, DMSci, kasper.karmark.iversen@regionh.dk

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2015

Primary Completion (Actual)

April 1, 2016

Study Completion (Actual)

June 1, 2016

Study Registration Dates

First Submitted

February 24, 2016

First Submitted That Met QC Criteria

February 28, 2016

First Posted (Estimate)

March 3, 2016

Study Record Updates

Last Update Posted (Estimate)

August 16, 2016

Last Update Submitted That Met QC Criteria

August 15, 2016

Last Verified

August 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • HerlevH02

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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