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WithdrawnNCT01444768CPOEUpdated Apr 5, 2017

Prospective Evaluation of Computerized Physician Order Entry in the Emergency Department

An observational study in Operational Metrics of the Emergency Department, sponsored by Beth Israel Deaconess Medical Center. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-04-05.

Sponsored by Beth Israel Deaconess Medical Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

This study will evaluate various performance metrics of emergency department operations after the implementation of computerized physician order entry in an academic emergency department.

Read the detailed description

The study will be a prospective before-after study comparing various operational and performance metrics before and after the implementation of a computerized physician order entry system in the emergency department.

The investigators will collect 6 month before, 6 month after of data along with a 2-4 week washout period. The investigators will also administer a computerized physician order entry survey after the study is completed. This confidential survey will be emailed to all ED nurses, residents, and attendings using RedCap. Consent will be implied if they choose to participate.

02

Conditions studied

  • Operational Metrics of the Emergency Department

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Keywords

  • Alert Systems, Medication
  • Computerized Physician Order Entry System
  • CPOE
  • Medication Alert Systems
  • Medical Order Entry Systems
03

In context

Emergencies

1,691 studies on the registry are indexed under Emergencies; 332 are open to participants now.

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Lead sponsor

Beth Israel Deaconess Medical Center is the lead sponsor of 560 studies on the registry; 80 are open to participants now.

Of its 75 completed or terminated interventional studies of FDA-regulated products, 61 (81%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients who are registered in the emergency department > 18 years of age who do not elope, left without being seen, or leave AMA.

Inclusion criteria

  • All consecutive adult patients (Age >=18) presenting to the Emergency Department during the study period will be included in the study.

Exclusion criteria

Exclusion Criteria:

  • Patients who eloped, left without being seen, or signed out against medical advice will be excluded.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)

Interventions

  • OtherComputerized Physician Order Entry

    Computer ordering system allowing emergency department physicians to order medications, laboratory tests, radiology studies, and nursing interventions

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What researchers measure

Primary outcomes

  1. Time to Antibiotics

    Primary outcome measure is time to antibiotics. This is defined as the time patients are registered to the time they receive their first antibiotics for patients with an ED diagnosis of pneumonia.

    Time frame: 6 months

Secondary outcomes

  1. Emergency Department Length of Stay

    Secondary outcome measure is length of stay defined as the time from patient registration to time the patients leave the emergency department.

    Time frame: 6 months

  2. Lab turnaround time

    Lab turnaround time is defined as the time it takes from when the sample is collected to when the results are entered.

    Time frame: 6 months

  3. Resource Utilization

    Resource utilization defined as the number of CBC, Chem7, and troponin tests ordered.

    Time frame: 6 months

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Study locations

1 site
  • Beth Israel Deaconess Medical Center
    Boston, Massachusetts 02215, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 5, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01444768
Lead sponsor
Beth Israel Deaconess Medical Center
Responsible party
Steven Horng, MD (Instructor in Emergency Medicine, Beth Israel Deaconess Medical Center) — Principal investigator
First posted
Oct 3, 2011
Start date
Mar 2012
Primary completion
Dec 2012 (estimated)
Completion
Dec 2013 (estimated)
Last update
Apr 5, 2017

Study contacts

Steven Horng, MD
principal investigator · Beth Israel Deaconess Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Apr 2017. You cannot join it, but the record below documents what was studied.

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