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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04069403
Other study ID # Pro00102219
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 10, 2019
Est. completion date June 15, 2020

Study information

Verified date April 2020
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Analyze baseline concurrent opioid prescribing metrics at the individual prescriber level in the Duke Health System on the identified three main outcome measures.

Test the impact of reports on opioid prescriber behaviors with the following primary measures: number of prescriptions with concurrent benzo within reporting period, number of prescriptions with concurrent muscle relaxants within reporting period, and number of encounters with naloxone prescriptions for patients with any opioid-related diagnosis within reporting period.

Create a blueprint to implement the concurrent opioid prescribing nudge intervention in other settings.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Other:
Automated Reports on prescription patterns for their patients
de-identified aggregate reports

Locations

Country Name City State
United States Duke University Medical Center Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Opioid prescribing habits Using baseline concurrent opioid prescribing metrics obtained (at the individual prescriber level) during their initial month and month prior in the Duke Health System, measure changes in Opioid n prescription orders as measured by provider prescriptions Baseline, 6 Months
Primary number of prescriptions with concurrent benzo within reporting period Identify the number of prescriptions with concurrent benzo over 6 months 6 Months
Primary number of prescriptions with concurrent muscle relaxants within reporting period Identify the number of prescriptions with concurrent muscle relaxants over 6 months 6 Months
Primary number of encounters with naloxone prescriptions for patients with any opioid-related diagnosis within reporting period Identify the number of encounters with naloxone prescriptions for patients with any opioid-related diagnosis over 6 months 6 Months
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