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RECRUITING
NCT03630055
PHASE3

Rivaroxaban Post-Transradial Access for the Prevention of Radial Artery Occlusion

Sponsor: Ottawa Heart Institute Research Corporation

View on ClinicalTrials.gov

Summary

Coronary angiography is performed to evaluate for obstructive coronary artery disease. This is commonly performed via the transfemoral or transradial approach with the latter increasing in frequency. One of the most common complications of transradial access is radial artery occlusion occurring in \~5% of patients which prohibits the use of the radial artery in the future. There is evidence to support the use of intraprocedural anticoagulation to mitigate the risk of radial artery occlusion however the role of post-procedural anticoagulation has not been previously evaluated. Rivaroxaban is a direct oral anticoagulant (DOAC) with a safety profile superior to that of vitamin K antagonists. Given the safety profile, ease of use, and feasibility of DOAC therapy, our study will endeavor to evaluate the use of rivaroxaban 15mg orally once daily for 7 days after transradial access and the impact this has on the rate of radial artery occlusion.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

1800

Start Date

2018-10-03

Completion Date

2026-06-30

Last Updated

2025-05-15

Healthy Volunteers

No

Interventions

DRUG

Rivaroxaban 15 MG Oral Tablet [Xarelto]

Patients will receive rivaroxaban 15mg orally daily for 7 days following transradial access.

Locations (3)

Mayo Clinic

Rochester, Minnesota, United States

Kingston Health Sciences Center

Kingston, Ontario, Canada

University of Ottawa Heart Institute

Ottawa, Ontario, Canada