- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00713297
Implementation of a Novel Computerized Physician Order Entry System
July 9, 2008 updated by: National Taiwan University Hospital
Implementation of a Novel Computerized Physician Order Entry System to Reduce Medication Errors
The objective of this prospective study is to build a real-time interactive platform where doctors and pharmacists may communicate and solve patients' drug-related problems (DRP) immediately and document accordingly.
This study will also design a computerized physician order entry (CPOE) system utilizing default protocol for chemotherapy order entry.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
To err is human.
Most errors are caused by problems in the system.
Punishing health personnel cannot prevent the same mistakes.
The only solution is a good medication system.
CPOE system can prevent prescribing errors.
The CPOE system is always the major step in some studies concerning reducing prescribing errors, dispensing errors or administering errors.
In this user-friendly and convenient era, improvement in the CPOE system is an immediate need.
Study Type
Observational
Enrollment (Anticipated)
80
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Fe-Lin L. Wu, MSCP,Ph D
- Phone Number: 8389 +886-2-23123456
- Email: flwu@ntu.edu.tw
Study Locations
-
-
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Taipei, Taiwan, 10051
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Fe-Lin L Wu, PhD
- Phone Number: 8389 +886-2-23123456
- Email: flwu@ntu.edu.tw
-
Principal Investigator:
- Fe-Lin L Wu, MSCP,PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
24 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
NTUH pharmacists
Description
Inclusion Criteria:
- NTUH pharmacists
Exclusion Criteria:
- NTUH pharmacists who have never recorded drug related problems
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Observation
Those who will use the new CPOE system
|
Satisfaction questionnaire
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
the timeliness and efficiency of pharmacist's response in DRPs, the average prescription error rate and the satisfaction questionnaire before and after implementation of the new CPOE system.
Time Frame: 2 year
|
2 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Fe-Lin L. Wu, MSCP,Ph D, Department of Pharmacy, N.T.U.H.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2007
Primary Completion (Anticipated)
December 1, 2008
Study Completion (Anticipated)
December 1, 2009
Study Registration Dates
First Submitted
July 9, 2008
First Submitted That Met QC Criteria
July 9, 2008
First Posted (Estimate)
July 11, 2008
Study Record Updates
Last Update Posted (Estimate)
July 11, 2008
Last Update Submitted That Met QC Criteria
July 9, 2008
Last Verified
June 1, 2008
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 200803060R
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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