NCT00713297

Brief Summary

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Sep 2007

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2007

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

July 9, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 11, 2008

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2008

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2009

Completed
Last Updated

July 11, 2008

Status Verified

June 1, 2008

Enrollment Period

1.3 years

First QC Date

July 9, 2008

Last Update Submit

July 9, 2008

Conditions

Computerized Physician Order Entry

Keywords

medication errorscomputerized physician order entrypharmaceutical carechemotherapeutic agentsreengineering

Outcome Measures

Primary Outcomes (1)

  • 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.

    2 year

Study Arms (1)

Observation

Those who will use the new CPOE system

Behavioral: satisfaction questionnaire

Interventions

satisfaction questionnaireBEHAVIORAL

Satisfaction questionnaire

Also known as: questionnaire
Observation

Eligibility Criteria

Age24 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

NTUH pharmacists

You may qualify if:

  • NTUH pharmacists

You may not qualify if:

  • NTUH pharmacists who have never recorded drug related problems

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University Hospital

Taipei, 10051, Taiwan

RECRUITING

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Fe-Lin L. Wu, MSCP,Ph D

    Department of Pharmacy, N.T.U.H.

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Fe-Lin L. Wu, MSCP,Ph D

CONTACT

+886-2-23123456flwu@ntu.edu.tw

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

July 9, 2008

First Posted

July 11, 2008

Study Start

September 1, 2007

Primary Completion

December 1, 2008

Study Completion

December 1, 2009

Last Updated

July 11, 2008

Record last verified: 2008-06

Locations

TW(1)