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Critical IllnessNCT01243021

Validation of an Early Warning Score Based Triage System in the Emergency Department

An observational study of Critical Illness, run by Bispebjerg Hospital at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

At Bispebjerg Hospital we have introduced an Early Warning Score based triage system , called Bispebjerg Early Warning Score (BEWS), in order to identify critically ill patient on arrival at the emergency department. The purpose of this study is to validate our triage system. Read more about this study

Who is it for?
Any age
Conditions the study is for
Critical Illness
How many people
300 participants
Where
1 siteDenmark
Study dates
Apr 2009to Sep 2009
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: When arriving at the emergency department patients are divided into on of three groups (red, blue nd white) according to the severity of their condition based on common regional guidelines. Red patients are the most servelery ill or injured patients. A random sample of "red" patients are included in this study

Who may be able to join

  • "Red" patient
  • Seen in our emergency department between 1. april 2009 and 30. september 2009

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Bispebjerg Hospital

    Copenhagen, Copenhagen NV, 2400

Other trials in Denmark

About this study

Official title: Nurse Administered Early Warning Score System Can be Used for Emergency Department Triage

At Bispebjerg Hospital we have introduced an Early Warning Score based triage system , called Bispebjerg Early Warning Score (BEWS), in order to identify critically ill patient on arrival at the emergency department. The purpose of this study is to validate our triage system.

Medical subject headings
Critical Illness

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Critical illness

    The investigators have defined a critically ill patient as a patient who dies within 48 hours of arrival at the emergency department or who is admitted to ICU within 48 hours of arrival at the emergency department

    Measured: 48 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Nov 2010 (estimated)
  2. Study startApr 2009
  3. Primary completionSep 2009
  4. Study completionSep 2009

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
300 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01243021
Sponsor's protocol ID
BBH98765
Status last verified
Nov 2010
First submitted
17 Nov 2010
Last updated
18 Nov 2010
Results posted
No
Data monitoring committee
No

Publications

  • Christensen D, Jensen NM, Maaloe R, Rudolph SS, Belhage B, Perrild H. Nurse-administered early warning score system can be used for emergency department triage. Dan Med Bull. 2011 Jun;58(6):A4221.

    PubMed 21651873

Questions about this trial

What is this clinical trial studying?

An observational study of Critical Illness, run by Bispebjerg Hospital at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Nov 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Critical illness (time frame: 48 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01243021, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Nov 2010.

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