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临床试验/NCT06212050
NCT06212050Enrolling By Invitation不适用

Investigator Initiated Multicenter Study to Evaluate the Feasibility, Safety and Effectiveness of the ACURATE neo2 Transcatheter Heart Valve for Severe Bicuspid Aortic Stenosis - The Neo2 BAV Registry

National University of Ireland, Galway, Ireland3 个研究点 分布在 3 个国家目标入组 200 人开始时间: 2023年9月15日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
200
试验地点
3
主要终点
VARC-3 device success

研究概览

简要总结

The goal of the NEO2 BAV registry is to investigate the safety, effectiveness, and clinical performance of TAVI using the ACURATE neo2 valve in patients with severe BAV stenosis.

The clinical, procedural, and imaging characteristics will be collected from patients with severe BAV stenosis, regardless of the phenotype, and treated with TAVI using the ACURATE neo2 bioprosthesis worldwide.

详细描述

As the use of TAVI in BAV anatomy expands, it is important to systematically evaluate clinical outcomes from various THV technologies among BAV patients. It is essential to consider short-, and longer-term events among patients with BAV undergoing TAVI. Short-term outcomes of interest include THV embolization, PVL, residual transvalvular gradients and patient prosthesis mismatch, aortic root rupture, the requirement for new PPI, and stroke. Longer-term term clinical events of interest include quality of life, THV durability, freedom from reintervention, maintained coronary access, the possibility of redo-TAVI, and mortality.

The ACURATE neo2 THV has design features that make it possible to successfully treat severe BAV stenosis and yield optimal short- and longer-term outcomes. A new active sealing skirt is designed to minimize residual PVL; this is especially relevant given the presence of severe calcifications in BAV. The supra-annular leaflet position is also likely to provide excellent haemodynamics and durability since they sit above the heavily calcified native valve leaflet calcification. The upper crown and stabilizing arches and the top-down deployment of the ACURATE neo2 should reduce the risk of device embolization. It is unclear however if the self-expanding frame of the neo2 has the optimal radial force to treat patients with severe calcification.

The plan is to collect systematic clinical, procedural, and imaging data on a large series of patients with severe symptomatic BAV stenosis who underwent TAVI using the ACURATE neo2 THV. This information will show if the ACURATE neo2 is suitable to treat BAV morphology and determine if there are specific BAV subtypes that are more suitable for alternative treatment strategies. It is also envisaged that this study will inform the procedural execution of ACURATE neo2 THV in BAV morphology and inform future iteration design of the ACURATE neo THV series.

All imaging data (Echocardiography, angiography, aortography and MSCT) will be meticulously analyzed in an independent imaging Core Lab (CORRIB Core Lab, University of Galway, Galway, Ireland).

The in-depth imaging analysis will allow the identification of patients that are suitable for TAVI using the ACURATE neo2 system and highlight patient or procedural features that render TAVI at elevated risk of adverse outcomes. Furthermore, a mechanistic understanding of the device-host interaction will be examined on post-TAVI multislice computed tomography (MSCT) and other available post-TAVI imaging studies.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged ≥ 18 years
  • Patients with severe AS and any BAV phenotype and indicated for TAVI based on the local heart team decision.
  • Patient treated with ACURATE neo2 THV.

排除标准

  • Failure to obtain the patient's consent
  • Failure to obtain the follow-up clinical data or cardiac imaging required for the study primary endpoints.

结局指标

主要结局

VARC-3 device success

时间窗: 30-Day

1. Number of patients with technical success. 2. Number of patients with death from any cause. 3. Number of patients with surgery or intervention related to the device or to a major vascular or access-related or cardiac structural complication. 4. Number of patients with intended performance of the valve (mean gradient \<20 mmHg, peak velocity \<3 m/s, Doppler velocity index ≥0.25, and less than moderate AR), defined as the presence of all of the following:

VARC-3 early safety

时间窗: 30-Day

1. Number of patients with death from any cause. 2. Number of patients with stroke. 3. Number of patients with VARC type 2-4 bleeding. 4. Number of patients with major vascular, access-related, or cardiac structural complication. 5. Number of patients with acute kidney injury stage 3 or 4. 6. Number of patients with moderate or severe aortic regurgitation 7. Number of patients with new pacemaker due to procedure related conduction abnormalities 8. Number of patients with surgery or intervention related to the device

次要结局

  • VARC-3 clinical efficacy (at 1 year and thereafter)(1-year)
  • Valve-related long-term clinical efficacy (at 5 years and thereafter)(5-year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Professor Osama SOLIMAN

Professor of Cardiovascular Research

National University of Ireland, Galway, Ireland

研究点 (3)

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