Actively Recruiting
Radial Access Data in Vascular Interventions: A Prospective Observational Registry Study
Led by Mersin Medicalpark Hastanesi · Updated on 2026-06-01
20000
Participants Needed
1
Research Sites
20 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The RADIUS study is a prospective observational registry focused on collecting real-world data about radial and ulnar artery access during percutaneous vascular interventions. It aims to evaluate procedural details, access-site complications, procedural success, and short-term clinical outcomes associated with these access methods. The study highlights the growing use of radial and ulnar access techniques as alternatives to traditional femoral access, given their potential benefits in patient safety and comfort. Patients undergoing routine percutaneous vascular interventions via radial or ulnar artery access at Mersin Medical Park Hospital will be consecutively enrolled from May 2026 through May 2031. The registry collects demographic, clinical, angiographic, procedural, and post-procedural data as part of standard clinical care. Expansion to multiple centers is planned following regulatory approvals, but no experimental treatments or devices are involved. Participants will have data collected from procedural reports, hospital records, and clinical evaluations covering variables such as cardiovascular risks, comorbidities, procedural duration, fluoroscopy time, contrast volume, and complications. Researchers will monitor outcomes including radial artery occlusion, spasm, vascular complications, procedural success, crossover rates, bleeding, length of hospital stay, and more for up to one year after the procedure. The study is purely observational and integrates with routine care without altering treatment plans.
CONDITIONS
Brief Title
Radial Access Data in Vascular Interventions Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Undergoing routine percutaneous vascular interventions via radial or ulnar artery access
- Ability to provide informed consent
You will not qualify if you...
- Under 18 years of age
- Procedures performed without radial or ulnar artery access
- Incomplete procedural or clinical data
- Refusal to participate in the registry
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 year after the procedure
Participants who undergo routine percutaneous vascular interventions via radial or ulnar artery access are observed. Data on procedural characteristics, vascular complications, and clinical outcomes are collected from procedural reports, hospital records, and routine clinical evaluations.
Assessments during hospital stay and follow-up visits up to 1 year
Trial Site Locations
Total: 1 location
1
Mersin Medicalpark hospital
Mersin, Mezitli, Turkey (Türkiye), 33010
Actively Recruiting
Research Team
S
Sefa SURAL, MD
G
Gökhan AVCI, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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