Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07399392

Radial Versus Femoral Secondary Access in Patients Undergoing TAVI

Led by University Heart Center Freiburg - Bad Krozingen · Updated on 2026-02-10

434

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Severe symptomatic aortic stenosis (AS) with a high gradient is associated with a poor prognosis if not treated with valve replacement. Transcatheter aortic valve implantation has been shown in large randomized trials to be a safe and effective treatment option for patients at low, intermediate, or high risk. Transfemoral access for heart valve replacement is by far the most commonly used approach, as it is relatively easy to control and has a low complication rate compared to other access routes. The TAVI procedure requires two arterial access points: one with a large lumen for the TAVI prosthesis via the femoral artery, and a smaller second one for a pigtail catheter that guides the TAVI prosthesis into the optimal position. This secondary access is most often via a second artery. Vascular complications are the most commonly observed complications in transfemoral TAVI and are associated with poorer procedural outcomes. Recent data suggest that secondary vascular access via the radial artery may contribute to a reduction in vascular complications after TAVI. In patients undergoing coronary angiography and/or percutaneous coronary intervention, radial access has become the preferred strategy due to its proven reduction in vascular complications compared to femoral access. The use of radial access is associated with a lower incidence of vascular complications compared to femoral access. Recent non-randomized data suggest that radial access may be a safer alternative to traditional femoral access as a secondary arterial access in transfemoral TAVI. However, non-randomized retrospective comparisons are subject to selection bias and underreporting of complications. Therefore, a prospective randomized trial is needed to evaluate the value of radial access for secondary arterial access in patients undergoing transfemoral TAVI.

CONDITIONS

Official Title

Radial Versus Femoral Secondary Access in Patients Undergoing TAVI

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for transfemoral TAVI
  • Heart team agrees on eligibility of TAVI
  • Written informed consent
  • Age > 18 years
Not Eligible

You will not qualify if you...

  • Radial arteries not accessible as judged by the TAVI team
  • Femoral arteries not accessible as judged by the TAVI team
  • Foreseeable problems to achieve primary transfemoral access (hostile access)
  • Hemodynamic instability or cardiogenic shock
  • Currently participating in an investigational drug or device study
  • Lack of capability to give informed consent
  • Patient refuses TAVI

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Heart Center - Deparment for Cardiology and Angiology

Freiburg im Breisgau, Germany, 79106

Actively Recruiting

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Research Team

C

Constantin von zur Muehlen, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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