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Evaluation of Electronic Prescribing in Hospital Ambulatory Care Clinics

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ClinicalTrials.gov Identifier: NCT00252395
Recruitment Status : Completed
First Posted : November 11, 2005
Last Update Posted : November 11, 2005
Sponsor:
Collaborator:
Health Canada
Information provided by:
Sunnybrook Health Sciences Centre

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.


Condition or disease Intervention/treatment Phase
Electronic Prescribing Device: PDA-based Electronic Prescribing Software Phase 4

Study Type : Interventional  (Clinical Trial)
Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Educational/Counseling/Training
Official Title: Effects of Electronic Prescribing on Safety and Quality in Hospital-Based Ambulatory Are: a Randomised Controlled Trial
Study Start Date : August 2005
Study Completion Date : August 2006

Resource links provided by the National Library of Medicine





Primary Outcome Measures :
  1. Total prescribing error, as measured by the number of call backs received from pharmacists.

Secondary Outcome Measures :
  1. a) Interactions
  2. b) Dosing and route of administration errors
  3. c) Pack errors
  4. d) Legibility errors


Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • inadequate prescribing practice (minimum number)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00252395


Locations
Canada, Ontario
Sunnybrook & Women's College Health Science Centre
Toronto, Ontario, Canada, M4N 3M5
Sponsors and Collaborators
Sunnybrook Health Sciences Centre
Health Canada
Investigators
Study Director: Merrick F Zwarenstein, MBBCH Institute for Clinical Evaluative Science
Principal Investigator: William J Sibbald, MD, MPH Sunnybrook & Women's College Health Sciences Centre

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00252395     History of Changes
Other Study ID Numbers: S&W e-RX
6804-15-2003/5590024
First Posted: November 11, 2005    Key Record Dates
Last Update Posted: November 11, 2005
Last Verified: November 2005

Keywords provided by Sunnybrook Health Sciences Centre:
medication error
electronic prescribing
patient safety