Specialty Hospital
Amman, Shmeisani, Jordan
NCT Number: NCT07138170
Background: Radial artery occlusion (RAO) is a recognized complication of transradial coronary access, with reported incidence rates ranging from 5% to 30%. Distal radial access (DRA), performed at the anatomical snuffbox, has emerged as a promising alternative that may better preserve radial artery patency by maintaining antegrade perfusion through the palmar arch during hemostasis.
Objective: To compare distal radial access with conventional transradial access in terms of radial artery patency and access-site outcomes in a real-world all-comers population undergoing coronary angiography or percutaneous coronary intervention.
Methods: This prospective, multicenter, open-label, quasi-randomized comparative study enrolled 350 patients across three community-based hospitals in Palestine and Jordan between 2024 and 2026. Patients were allocated in a 1:1 ratio to DRA (n=183) or conventional transradial access (n=167) using an alternating sequence. The primary endpoint was radial artery patency assessed by blinded duplex ultrasonography at 24 hours and at 1 to 6 months. Secondary endpoints included access-site pain, bruising, numbness, and crossover to an alternative access site. The 24-hour outcome was analyzed by intention-to-treat and long-term outcomes by per-protocol analysis. Adjusted analyses used Firth penalized logistic regression.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Amman, Shmeisani, Jordan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Using Conventional Transradial Artery Access for Cardiac Catheterization
Using Distal Radial Artery access for Cardiac Catheterization
Time frame: 24 hours and 1-6 months post procedure
Radial artery occlusion defined as absence of antegrade flow on duplex ultrasonography, assessed within 24 hours and at 1-6 months after the procedure.
Time frame: 24 hours and 1-6 months post-procedure.
The patients will be asked to rate their pain on a 1-10 scale.
Time frame: At the time of procedure
In cases where radial access is unsuccessful, crossover to an alternative access site, such as the contralateral radial or femoral artery, will be documented
Time frame: 24 hours and 1-6 months post-procedure
Number of participants with numbness at the access site assessed by physical examination.
Time frame: 24 hours and 1-6 months post-procedure
Number of participants with bruising at the access site assessed by physical examination.
Jordanian Research and Artificial Intelligence Group
Other
Comparison of Distal and Conventional Transradial Access for Coronary Catheterization: A Multicenter, Quasi-Randomized Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.