Bicuspid Aortic Valve Replacement: Evaluation of Transcatheter Versus Surgery-Pilot Trial (BELIEVE-IT)

Cedars-Sinai Medical Center

Status: Enrolling

Conditions: Bicuspid Aortic Valve; Aortic Valve Stenosis

Treatments: Procedure: surgical aortic valve replacement (SAVR); Procedure: transcatheter aortic valve replacement (TAVR)

Study type: Interventional

Funder types: Other

Identifiers

NCT06817148

STUDY00003805

Details and patient eligibility

About

The study protocol is a randomized trial of standard of care therapies for severe aortic stenosis (AS) in patients with a bicuspid aortic valve (BAV). Namely, the therapies to which patients will be randomized will be transcatheter aortic valve replacement (TAVR) or surgical aortic valve replacement (SAVR), in patients deemed clinically suitable for both following heart team review.

The purpose of this study is to compare the safety and efficacy of Transcatheter Aortic Valve Replacement (TAVR) versus Surgical Aortic Valve Replacement (SAVR) for treating patients with severe aortic stenosis (AS) who have a congenital bicuspid aortic valve (BAV) anatomy. Patients with BAV anatomy have been under-represented in previous trials and this study might provide important information to help guide future treatment options.

The study patients will be followed with standard of care procedures for 10 years.

Enrollment: 250 estimated patients

Sex: All

Ages: 50+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Provision of signed and dated informed consent form
• Stated willingness to comply with all study procedures and availability for the duration of the study
• Male or female, aged > 50 years of age
• Site-determined severe AS deemed necessary for treatment with SAVR or TAVR
• Gated contrast CT available and suitable for core laboratory analysis
• BAV anatomy confirmed by CT core laboratory analysis

Exclusion criteria

• Recent cardiovascular intervention within the prior 30 days.
• Presence of an existing TAVR or SAVR device
• Pregnancy or lactation
• Extreme or prohibitive TAVR or SAVR risk, determined by site or committee Active enrollment in another investigational study
• Disproportionate TAVR vs SAVR risk, as determined by treating site or committee
• Associated aortopathy (AA≥ 45 mm by maximal cross-sectional dimension, as confirmed by CT core laboratory analysis, or AA<45 mm but site plan for surgery of the aorta in the event of randomization to surgery
• Site plan for treatment of concomitant non-coronary cardiovascular disease in the event of randomization to surgery (for instance, concomitant valve surgery, septal defect or coarctation repair, aorta or root replacement or repair)
• In the presence of coronary artery disease deemed necessary for revascularization in the event of randomization to SAVR or TAVR, Syntax score ≥ 32 or deemed unsuitable for PCI, or deemed unsuitable for coronary artery bypass grafting (CABG).

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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250 participants in 2 patient groups

transcatheter aortic valve replacement (TAVR)

Active Comparator group

Description:

50% of patients will be treated with standard TAVR procedure and followed up for 10 years

Treatment:

Procedure: transcatheter aortic valve replacement (TAVR)

surgical aortic valve replacement (SAVR)

Active Comparator group

Description:

50% of patients will be treated with standard SAVR procedure and followed up for 10 years

Treatment:

Procedure: surgical aortic valve replacement (SAVR)