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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02223676
Other study ID # 1-16-02-379-13
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2013
Est. completion date December 2014

Study information

Verified date August 2014
Source Randers Regional Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effect of implementing clinical pharmacists in the Emergency Department Team at Randers Regional Hospital. The clinical pharmacists conduct medication history, make medical interaction screenings, -reconciliations and -reviews on unscheduled patients admitted to the Emergency Department during daytime.


Recruitment information / eligibility

Status Completed
Enrollment 448
Est. completion date December 2014
Est. primary completion date June 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- unscheduled patients admitted to the Emergency Department at Randers Regional Hospital at weekdays during daytime (9 am to 16.15 pm)

- 4 or more drugs prescribed

Exclusion Criteria:

- patients triage red

- patients who cannot give informed consent

- terminal patients

- patients admitted to detoxification

- patients refered to the acute outpatient department

- patients remaining in the Emergency Department overnight

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Clinical pharmacists conduct medication history
pharmacists conduct medication history before the physician interviews the patient and does not spend time on conducting medical history

Locations

Country Name City State
Denmark Randers Regional Hospital Randers Region Midt

Sponsors (2)

Lead Sponsor Collaborator
Randers Regional Hospital Aarhus University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other The impact of the intervention in the Emergency Department on the existing medication review by clinical pharmacist at the acute ward We estimate whether the intervention is time-saving (by recording and comparing time spent for secondary/excisting medication review at the acute ward between patients allocated to the intervention and control group, respectively) and reduce the workload of the clinicians (number and kind of interventions at secondary medication review in the two groups) 1-3 days after admission to Emergency Department when the secondary medication review takes place
Other The impact of the intervention in the Emergency Department on the dispensing of medicine (done by nurses) time used and the possibility of substitutions During actual admission to the Emergency Department and the period after inclusion of patients
Primary Emergency Department Length of stay From arrival to the Emergency Department to either admission or discharge, which in average will be 6 hours.
Secondary Time from patient arrival to the treatment schedule is ready From arrival to the Emergency Department to either admission or discharge, which in average will be 6 hours.
Secondary Patient safety Number of recommended changes in drugs or dosage per patient. The changes are rated according to a PCNE-classification for drug-related problems. From arrival to the Emergency Department to either admission or discharge, which in average will be 6 hours.
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