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Study identifier: NCT06232551 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Alerting Providers at Patient Hospital Discharge to Consider Prescribing Rivaroxaban to Reduce Venous Thromboembolism

Condition: Venous Thromboembolic Disease · Pulmonary Embolism and Thrombosis · Deep Vein Thrombosis  ·  Sponsor: Scott C. Woller, MD

PhaseNA
Planned participants152000
Who can joinAll sexes, 18 Years to 110 Years
Healthy volunteersNo

About this study

A new algorithm derived from only patient age and components of the complete blood count and basic metabolic panel can identify patients discharged from the hospital who may benefit from a blood thinner (called rivaroxaban) to decrease their risk of blood clots, and for whom the risk of bleeding is minimal. The purpose of this study is to evaluate the use of a pop-up alert, which will be seen by clinicians when a discharging patient has been identified as being someone for whom the risk of blood clots is high, but for whom bleeding risk is estimated to be low. The pop-up alert will be enabled in a sequential fashion for each group of hospitals in 1 month blocks. We will look to see if the pop-up alert changes the number of patients who receive rivaroxaban. We will also measure the outcomes of blood clots and bleeding among all discharging patients.

This description comes directly from the study's public registry record.

Talk to the study team

Valerie Aston, MBA  ·  801-507-4606  ·  valerie.aston@imail.org

Carlos Barbagelata, MS  ·  801-507-4607  ·  carlos.barbagelata@imail.org

Always discuss trial participation with your own doctor first.

Locations (1)

Intermountain Medical CenterMurray, Utah, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06232551