TRanscatheter Aortic-Valve Implantation Without On-site Cardiac Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorUniversity Hospital of Ferrara

About this trial

TRACS-PRIME is a prospective, randomized, multicenter clinical trial evaluating whether transcatheter aortic valve implantation (TAVI) can be performed safely and effectively in selected hospitals without on-site cardiac surgery, when appropriate patient selection, experienced operators, advanced imaging, and established transfer pathways are available. The study will include patients with severe symptomatic aortic stenosis who have an indication for TAVI confirmed by a multidisciplinary Heart Team. Eligible patients will be randomized to undergo TAVI either in a center without on-site cardiac surgery or in a center with on-site cardiac surgery. All procedures will be performed according to current standards of care by experienced TAVI operators. The main purpose of the study is to determine whether TAVI performed in centers without on-site cardiac surgery is not inferior to TAVI performed in centers with on-site cardiac surgery with respect to clinical outcomes at 1 year. The primary clinical outcome includes death from any cause, stroke, or hospitalization related to the procedure or the implanted valve. The study will also assess safety outcomes, including valve-related death and major procedural or technical complications. Participants will be followed after hospital discharge to assess clinical events, safety, and longer-term outcomes. An independent committee blinded to treatment allocation will review clinical events, and an independent Data Safety Monitoring Board will monitor patient safety during the trial.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Severe aortic stenosis

Indication to TAVI confirmed by the Heart Team

Prohibitive operative risk

High surgical risk as defined as STS score >8%

Disqualifiers

Unsuitable for transfemoral TAVI

Emergent TAVI

Non-cardiovascular comorbidity reducing life expectancy to <1 year

Any factor precluding 1-year follow-up

Trial design

Design model

Parallel

Treatments tested in this trial

  • Transcatheter Aortic Valve Implantation

    Procedure/Surgery

    Transcatheter aortic valve implantation is performed as the study procedure in patients with severe aortic stenosis and an indication for TAVI confirmed by the multidisciplinary Heart Team. The procedure is performed according to current guidelines and institutional standards by experienced TAVI operators. In this trial, the intervention is evaluated according to the setting in which it is performed: either in a center without on-site cardiac surgery or in a center with on-site cardiac surgery.

Treatment groups

1,612 Participants
are divided into 2 treatment groups
Group A: TAVI in center without on-site cardiac surgeryExperimental treatment 1 intervention
Group B: TAVI in center with on-site cardiac surgeryActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

all-cause mortality, all stroke, or hospitalization for procedure- or valve-related causes

The primary clinical efficacy outcome is a composite endpoint defined as the occurrence of any of the following events within 1 year after randomization: death from any cause, any stroke, or hospitalization related to the TAVI procedure or to the implanted valve. This endpoint will be assessed prospectively and adjudicated by an independent Clinical Events Committee blinded to treatment allocation.

Time frame
1-year

Secondary outcomes

1

All-cause death

Time frame
1-year
2

Cardiovascular death

Time frame
1-year
3

All stroke

Time frame
1-year
4

Ischemic stroke

Time frame
1-year

Other outcomes

1

Valve-related mortality, cardiac structural complications or other acute procedural and technical valve-related complications

The primary safety outcome is a composite endpoint defined as the occurrence within 1 year of any of the following events: valve-related mortality, cardiac structural complications, or other acute procedural and technical valve-related complications. Events will be defined according to VARC-3 criteria and adjudicated by an independent Clinical Events Committee blinded to treatment allocation.

Time frame
1-year

Sponsors and contacts

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University Hospital of Ferrara

Lead sponsor

Consorzio Futuro in Ricerca

Collaborator