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Evaluation of Electronic Prescribing in Hospital Ambulatory Care Clinics

Effects of Electronic Prescribing on Safety and Quality in Hospital-Based Ambulatory Are: a Randomised Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00252395
Enrollment
40
Registered
2005-11-11
Start date
2005-08-31
Completion date
2006-08-31
Last updated
2005-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Electronic Prescribing

Keywords

medication error, electronic prescribing, patient safety

Brief summary

All reliably evaluated POE systems to date have been desktop computer based, but now there is widespread use and acceptance among physicians of PDA devices for a variety of purposes. Clinicians report that drug information on a PDA improved their access to information and efficiency while reducing their self perceived error rates6. The use of these devices for information retrieval in clinical settings is expected to grow as wireless communication becomes more ubiquitous and as more applications become available6,7. During the past decade there has been a growing awareness of several issues aimed at promoting safer health care for our patients - point of care information technology is one of the keys. To this end we have worked with a Canadian company, Drugmagnet, to develop and implement PDA-based electronic prescribing system within a major Canadian academic health centre. This is a cluster randomised trial, in which access to and use of the e-prescribing system is switched on and off for randomly chosen weeks, thus time serves as the randomized element.

Interventions

DEVICEPDA-based Electronic Prescribing Software

Sponsors

Health Canada
CollaboratorOTHER_GOV
Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
ECT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
0 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* active staff physician at Sunnybrook & Women's College HSC

Exclusion criteria

* inadequate prescribing practice (minimum number)

Design outcomes

Primary

MeasureTime frame
Total prescribing error, as measured by the number of call backs received from pharmacists.

Secondary

MeasureTime frame
a) Interactions
b) Dosing and route of administration errors
c) Pack errors
d) Legibility errors

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 6, 2026