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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01573195
Other study ID # 2012-0168 (MSN141105)
Secondary ID Merk Dr Fox
Status Completed
Phase Phase 4
First received May 4, 2011
Last updated December 16, 2014
Start date March 2011
Est. completion date April 2012

Study information

Verified date December 2014
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to pilot the use of best practices alerts to enhance an antimicrobial stewardship program using the electronic medical record, EPIC.


Description:

The purpose of this study is to pilot the use of best practices to enhance an antimicrobial stewardship program using the electronic medical record, EPIC. Screening information technology tools via SETNET/Safety SUrveyor(Premier) and the electronic anti-infective order form would allow for sufficient medical record review to create best practices alerts for the purpose of appropriate de-escalation of anti-invectives.


Recruitment information / eligibility

Status Completed
Enrollment 1285
Est. completion date April 2012
Est. primary completion date April 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Physicians with prescribing privileges at the UWHC

Exclusion Criteria:

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Wisconsin Hospitals and Clinics Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

References & Publications (1)

Schulz L, Osterby K, Fox B. The use of best practice alerts with the development of an antimicrobial stewardship navigator to promote antibiotic de-escalation in the electronic medical record. Infect Control Hosp Epidemiol. 2013 Dec;34(12):1259-65. doi: 1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of best practice alerts(BPA) that were completely accepted, partially accepted, or rejected within 72 hours of issuing the BPA after issuing the BPA for deescalation, the responding healthcare provider will respond in one of the manners above One Year No
Secondary The number and type of antiinfectives that were administered before and after(11days) the best practice alert is issued. The antiinfective use before and after the BPA will be analyzed in detail. The number of antibiotics, percentage decrease(or less likely increase) in antiinfectives in the 3 days before BPA , and 11 days after the BPA will be analyzed. A cost analysis will be performed. Patient outcomes will not be assessed. One year No
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