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Radial Access Data in Vascular Interventions Registry

NCT07614386 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 20000

Last updated 2026-06-01

No results posted yet for this 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.

Conditions

  • Radial Artery Occlusion
  • Radial Artery Spasm
  • Vascular Access Complications
  • Coronary Artery Disease
  • Peripheral Arterial Disease

Interventions

PROCEDURE

Radial and Ulnar Artery Access

Routine percutaneous vascular interventions performed via radial or ulnar artery access according to standard clinical practice.

Sponsors & Collaborators

  • Mersin Medicalpark Hastanesi

    lead OTHER

Principal Investigators

  • Sefa SURAL, MD · Toros University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-15
Primary Completion
2030-12-31
Completion
2031-05-20

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07614386 on ClinicalTrials.gov