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Reduce Medication Errors by Translating AESOP Model Into CPOE Systems

T

Taipei Medical University

Status

Completed

Conditions

Hypertension

Treatments

Other: AESOP service system

Study type

Interventional

Funder types

Other

Identifiers

NCT03484793
NSC105-2634-F-038-001

Details and patient eligibility

About

Medication errors are common, life-threatening, costly but preventable. Information technology and automated systems are highly efficient for preventing medication errors and therefore widely employed in hospital settings. In this study, investigators would perform a cluster randomized controlled trial of a clinical reminding system that uses DNN and Probabilistic models to detect and notify physicians of inappropriate prescriptions, giving them the opportunity to correct these gaps and increase prescriptions completeness. This study aim is to assess whether or not this system would improve prescription notation for a broad array of patient conditions.

Full description

This paper focuses on "Big data" in the knowledge base, using "Data minig" study of DM (Disease-Medication) and MM (Medication-Medication) of relevance to develop associated decision resources system-"the intelligent safety system" (Advanced Electronic Safety of Prescriptions,AESOP Model), and test the system in the clinical environment in hospital can assist physicians when open orders reduce medication errors, the system is named "AESOP Model".

Enrollment

37 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Physicians who are working at the outpatient clinics in hospitals.
  • Physicians who sign the consent form

Exclusion criteria

  • Physicians who are unable to participate in this trial for the whole process
  • Physicians who do not sign the consent form

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

37 participants in 2 patient groups

AESOP integrated to CPOE for reducing medication errors
Experimental group
Description:
18 were assigned to the experimental group
Treatment:
Other: AESOP service system
Non AESOP
No Intervention group
Description:
19 were assigned to the traditional CPOE system

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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