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Pharmacist RecommendationsNCT01723462

How Often Are Pharmacist Recommendations Followed by Emergency Physicians in Emergency Departments?

An observational study of Pharmacist Recommendations, run by University of Southern Denmark 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

Clinical pharmacy has played a role in Emergency Departments (ED). The presence of pharmacists have been shown to reduce medication errors and improve the medication history taken at admission. Read more about this study

Who is it for?
Ages 15 years and older
Conditions the study is for
Pharmacist Recommendations
How many people
301 participants
Where
1 siteDenmark
Study dates
Aug 2008to Mar 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 15 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: all acute admissions to emergency department

Who may be able to join

  • all acute admissions to emergency department who were treated with one or more drugs

Who cannot join

  • children less than 15 years.

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Kolding Sygehus

    Kolding, 6000

Other trials in Denmark

About this study

Clinical pharmacy has played a role in Emergency Departments (ED). The presence of pharmacists have been shown to reduce medication errors and improve the medication history taken at admission. In Denmark a recent study revealed that clinical pharmacists identified medication problems in 25% of all admission to the ED, of which 47 % were considered to be serious.

However, the pharmacist recommendations are of little value if they are not acknowledged or followed by the physicians.

The aim of the present study was to analyze how often and under which circumstances the physicians made use of pharmaceutical recommendations in an ED with a mixed patient population with special attention to those recommendations, which were of significant or disastrous importance.

What is being measured

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

  1. number of pharmacist recommendations

    Measured: up to 48 hours after admission

Timeline

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

  1. First posted7 Nov 2012 (estimated)
  2. Study startAug 2008
  3. Primary completionMar 2009
  4. Study completionMar 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
Prospective
Enrolment
301 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01723462
Sponsor's protocol ID
SLB-ED-02-2012
Status last verified
Nov 2012
First submitted
5 Nov 2012
Last updated
8 Nov 2012
Results posted
No
Data monitoring committee
No

Publications

  • Mogensen CB, Olsen I, Thisted AR. Pharmacist advice is accepted more for medical than for surgical patients in an emergency department. Dan Med J. 2013 Aug;60(8):A4682.

    PubMed 23905567

Questions about this trial

What is this clinical trial studying?

An observational study of Pharmacist Recommendations, run by University of Southern Denmark 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 1 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 8 Nov 2012. 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?

number of pharmacist recommendations (time frame: up to 48 hours after admission). 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 NCT01723462, 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 8 Nov 2012.

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