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Radial Versus Femoral Secondary Access in Patients Undergoing TAVI

Radial Versus Femoral Secondary Access in Patients Undergoing TAVI

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07399392
Acronym
RADIAL-TAVI
Enrollment
600
Registered
2026-02-10
Start date
2025-07-01
Completion date
2028-12-31
Last updated
2026-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

TAVI(Transcatheter Aortic Valve Implantation)

Brief summary

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.

Interventions

PROCEDURERadial TAVI

patients will recieve the TAVI intervention via radial access

PROCEDUREfemoral TAVI

patients will recieve the TAVI intervention via femoral access

Sponsors

University Heart Center Freiburg - Bad Krozingen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients scheduled for transfemoral TAVI * Heart team agrees on eligibility of TAVI * Written informed consent * Age \> 18 years

Exclusion criteria

* Non accessible radial arteries as judged by the TAVI team * Non accessible femoral arteries 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 another device study * Lack of capability to give informed consent * Patient refuses TAVI

Design outcomes

Primary

MeasureTime frame
Vascular and bleeding complications related to the secondary vascular access site30 days

Secondary

MeasureTime frameDescription
Until 30 days after index procedure:30 days* cardiovascular mortality * non-cardiovascular mortality * mortality related to vascular and bleeding complications * Incidence of new neurological events after randomization * Vascular complications at 30 days * Bleeding complications at 30 days * Incidence of acute kidney injury

Countries

Germany

Contacts

CONTACTConstantin von zur Muehlen, MD
constantin.vonzurmuehlen@uniklinik-freiburg.de+49 761 270 34415

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 3, 2026