Clinical Trials Logo

Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01444768
Other study ID # 2011P000308
Secondary ID
Status Withdrawn
Phase N/A
First received September 29, 2011
Last updated April 4, 2017
Start date March 2012
Est. completion date December 2013

Study information

Verified date April 2017
Source Beth Israel Deaconess Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2013
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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:

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

Study Design


Related Conditions & MeSH terms

  • Emergencies
  • Operational Metrics of the Emergency Department

Intervention

Other:
Computerized Physician Order Entry
Computer ordering system allowing emergency department physicians to order medications, laboratory tests, radiology studies, and nursing interventions

Locations

Country Name City State
United States Beth Israel Deaconess Medical Center Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Beth Israel Deaconess Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 6 months
Secondary 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. 6 months
Secondary 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. 6 months
Secondary Resource Utilization Resource utilization defined as the number of CBC, Chem7, and troponin tests ordered. 6 months