Radial Access Data in Vascular Interventions Registry

Condition(s) studied

Investigational drug(s) / intervention(s)

Radial and Ulnar Artery Access: Routine percutaneous vascular interventions performed via radial or ulnar artery access according to standard clinical practice.

Study summary

The RADIUS study is a prospective observational registry designed to collect real-world data regarding radial and ulnar artery access in percutaneous vascular interventions. The study aims to evaluate procedural characteristics, access-site complications, procedural success, and short-term clinical outcomes associated with transradial and transulnar vascular access.

Patients undergoing routine percutaneous vascular interventions via radial or ulnar artery access at Mersin Medical Park Hospital will be consecutively enrolled. Demographic, clinical, angiographic, procedural, and post-procedural data will be prospectively collected and analyzed.

The study was initially designed as a single-center registry; however, following Institutional Review Board (IRB) approval, expansion into a multicenter registry with participating centers is planned.

This study is observational in nature and does not involve any experimental treatment, device, or intervention beyond standard clinical care.

Eligibility

Primary outcome measure(s)

• Radial Artery Occlusion Rate — Within 1 year after procedure
  Incidence of radial artery occlusion following percutaneous vascular interventions performed via radial artery access.
• Access-Site Vascular Complication Rate — through study completion, an average of 1 year
  Incidence of vascular access-site complications including bleeding, hematoma, pseudoaneurysm, arterial dissection, and vascular injury.
• Radial Artery Spasm Rate — During Procedure
  Incidence of clinically significant radial artery spasm during or immediately after the procedure.

Trial sites (1)

Other trials for the same condition