Post-Discharge Opioid Reduction Intervention for Open, Laparoscopic, and Endoscopic Surgery

Completed · Not applicable

Conditions studied: Prostate Cancer, Opioid Use

In brief

ORIOLES is a non-randomized, pre-post intervention study designed to improve quality of opioid prescribing and use after discharge for patients undergoing urologic surgery. The study will initially focus on a pre-defined cohort of patients undergoing radical prostatectomy. After the predefined study period for the pre-intervention arm, a three-part intervention is employed to assess the effect on opioid prescribing and use in the post-intervention arm. Pending results, the intervention may be applied to all surgeries in the department for routine clinical care.

Key facts

Study ID

NCT03536065

Run by

Johns Hopkins University

People needed

443

Starts

2017-08-01

Expected to finish

2019-03-01

Last updated by the study team

2020-07-28

Who can join

Age: 18 and older, up to 100. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• All patients diagnosed with prostate cancer and enrolled in NCT03006562

You may not qualify if…

• Patients not undergoing radical prostatectomy (for the primary pre-post ORIOLES study)

Where it is running

• Johns Hopkins Hospital — Baltimore, Maryland, United States

Full record on ClinicalTrials.gov

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