Implementation of a Novel Computerized Physician Order Entry System
Recruitment status was Recruiting
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Computerized Physician Order Entry |
Behavioral: satisfaction questionnaire |
| Study Type: | Observational |
| Study Design: | Observational Model: Ecologic or Community Time Perspective: Prospective |
| Official Title: | Implementation of a Novel Computerized Physician Order Entry System to Reduce Medication Errors |
- 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 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 80 |
| Study Start Date: | September 2007 |
| Estimated Study Completion Date: | December 2009 |
| Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Observation
Those who will use the new CPOE system
|
Behavioral: satisfaction questionnaire
Satisfaction questionnaire
Other Name: questionnaire
|
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.
Eligibility| Ages Eligible for Study: | 24 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
NTUH pharmacists
Inclusion Criteria:
- NTUH pharmacists
Exclusion Criteria:
- NTUH pharmacists who have never recorded drug related problems
Contacts and Locations| Contact: Fe-Lin L. Wu, MSCP,Ph D | +886-2-23123456 ext 8389 | flwu@ntu.edu.tw |
| Taiwan | |
| National Taiwan University Hospital | Recruiting |
| Taipei, Taiwan, 10051 | |
| Contact: Fe-Lin L Wu, PhD +886-2-23123456 ext 8389 flwu@ntu.edu.tw | |
| Principal Investigator: Fe-Lin L Wu, MSCP,PhD | |
| Principal Investigator: | Fe-Lin L. Wu, MSCP,Ph D | Department of Pharmacy, N.T.U.H. |
More Information
No publications provided
| Responsible Party: | Wu, Fe-Lin, Lin/Director, Department of Pharmacy, N.T.U.H. |
| ClinicalTrials.gov Identifier: | NCT00713297 History of Changes |
| Other Study ID Numbers: | 200803060R |
| Study First Received: | July 9, 2008 |
| Last Updated: | July 9, 2008 |
| Health Authority: | Taiwan: Department of Health |
Keywords provided by National Taiwan University Hospital:
|
medication errors computerized physician order entry pharmaceutical care chemotherapeutic agents reengineering |
ClinicalTrials.gov processed this record on May 19, 2013