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RECRUITING
NCT06812455
PHASE4

Effect of RIVAroxaban in Radial Artery Occlusion Treatment After Cardiac Catheterization

Sponsor: AHEPA University Hospital

View on ClinicalTrials.gov

Summary

The purpose of the RIVA-RAO study is to determine whether the use of Rivaroxaban is an effective treatment of radial artery occlusion (RAO) after cardiac catheterization (both angiography and PCI). This is a prospective, single-center, randomized controlled, open-label study that will randomize patients with RAO into two groups, one receiving Rivaroxaban and the other receiving no anticoagulation. RAO will be detected by radial artery ultrasound up to 24 hours after the procedure. Study objectives: Primary objective: To evaluate the effect of treatment with Rivaroxaban, in patients (both symptomatic and asymptomatic) with RAO after a coronary catheterization procedure (both angiography and percutaneous coronary intervention-PCI), in improving patency rates of the radial artery at 4 weeks after the procedure, compared with no-anticoagulation treatment. Secondary objectives: To compare local access site and systemic complications (bleeding events, pseudoaneurysm, arteriovenous fistula) at 4 weeks after the procedure between the two groups.

Official title: Effect of RIVAroxaban in Reducing Radial Artery Occlusion Rate After Transradial Coronary Catheterization

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2025-03-01

Completion Date

2029-03-01

Last Updated

2025-02-11

Healthy Volunteers

No

Interventions

DRUG

Rivaroxaban

Patients with RAO that will receive p.o. tabs Rivaroxaban 20 mg q.d.

Locations (1)

AHEPA University Hospital

Thessaloniki, Greece