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Evaluation of a Management Algorithm for TAVI Patients With Concomitant Mitral or Tricuspid Regurgitation (MASTER-TAVI II)

2026年5月28日 更新者:Josep Rodes-Cabau

Evaluation of a Treatment Algorithm for the Management of TAVI Patients With Significant Concomitant Mitral or Tricuspid Regurgitation

Aortic stenosis is a condition in which the aortic valve becomes narrow and does not open properly, making it harder for the heart to pump blood to the body. Transcatheter aortic valve implantation (TAVI) is a minimally invasive procedure commonly used to treat this condition, especially in older patients or patients at high surgical risk.

Many patients undergoing TAVI also have leakage of the mitral valve and/or tricuspid valve. These valve problems can cause symptoms such as shortness of breath, fatigue, swelling, heart failure, and repeated hospitalizations. Patients with multiple valve diseases generally have worse outcomes and are more difficult to treat.

In some patients, mitral or tricuspid valve leakage improves after TAVI because the heart works better once the aortic valve has been treated. However, in other patients, the leakage remains severe and continues to affect their health and quality of life. New minimally invasive treatments are now available to repair or replace the mitral and tricuspid valves, but doctors still do not know the best order or timing for these procedures.

This study aims to evaluate a treatment algorithm for patients with severe aortic stenosis and significant mitral and/or tricuspid valve leakage. The proposed approach follows current clinical guidelines and uses a stepwise strategy. Patients will first undergo TAVI, followed by reassessment of the mitral and tricuspid valves. If important valve leakage persists after TAVI, additional minimally invasive procedures may be considered to treat the mitral or tricuspid valve.

The study will include patients with severe aortic stenosis and moderate-to-severe or severe mitral and/or tricuspid regurgitation. Researchers will collect information about patient symptoms, heart imaging results, procedures, hospitalizations, quality of life, and clinical outcomes during follow-up.

The main goal of the study is to evaluate whether this staged treatment approach is safe, feasible, and effective in improving patient outcomes. Researchers will also assess whether the strategy can reduce hospitalizations for heart failure and improve symptoms, daily functioning, and quality of life.

The results of this study may help doctors better manage patients with multiple valve diseases and provide a more personalized and structured treatment approach for this complex group of patients.

研究概览

研究类型

观察性的

注册 (估计的)

300

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

The study population will consist of adult patients with severe symptomatic aortic stenosis undergoing transcatheter aortic valve implantation (TAVI) who also present with significant concomitant mitral regurgitation and/or tricuspid regurgitation. The study will mainly include elderly patients and patients considered at intermediate, high, or prohibitive surgical risk for conventional open-heart surgery.

Eligible participants will have moderate-to-severe or severe mitral and/or tricuspid valve regurgitation identified by echocardiography before TAVI. Patients will be evaluated and treated according to a staged transcatheter treatment algorithm based on current clinical guidelines and the evolution of valve disease following TAVI.

描述

Inclusion Criteria:

  • Age >18 years.
  • Patients with severe AS undergoing transarterial TAVI.
  • Concomitant significant MR and/or TR (≥3+).

Exclusion Criteria:

  • Life expectancy <1 year due to noncardiac conditions.
  • Any prior mitral or tricuspid valve surgery.
  • Echocardiographic evidence of intracardiac mass, thrombus, or vegetation.
  • Active endocarditis.
  • Subjects in whom transesophageal echocardiography is contraindicated or high risk.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Concomitant isolated MR - 3+ or 4
Patients with severe aortic stenosis (AS) and significant mitral regurgitation (MR) undergoing TAVI followed, if needed, by mitral intervention (M-TEER).
Concomitant isolated TR - 3+ to 5
Patients with severe AS and significant tricuspid regurgitation (TR) undergoing TAVI followed, if needed, by tricuspid intervention (T-TEER).
Concomitant MR and TR
Patients with severe AS, MR, and TR undergoing staged triple-valve transcatheter therapy.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
All-cause mortality or re-hospitalization for worsening heart failure
大体时间:Minimum of 1 year
Composite of all-cause mortality or re-hospitalization for worsening heart failure at a minimum of 1 year following the TAVI procedure
Minimum of 1 year

次要结果测量

结果测量
措施说明
大体时间
All-cause mortality or re-hospitalization for worsening heart failure
大体时间:1 Year
Composite of all-cause mortality or re-hospitalization for worsening heart failure at 1-year follow-up.
1 Year
All-cause mortality or re-hospitalization for worsening heart failure
大体时间:2 year
Composite of all-cause mortality or re-hospitalization for worsening heart failure at 2-year follow-up
2 year
All-cause mortality or re-hospitalization for worsening heart failure
大体时间:3 year
Composite of all-cause mortality or re-hospitalization for worsening heart failure at 3-year follow-up.
3 year
All-cause mortality or re-hospitalization for worsening heart failure
大体时间:4 year
Composite of all-cause mortality or re-hospitalization for worsening heart failure at 4-year follow-up.
4 year
All-cause mortality or re-hospitalization for worsening heart failure
大体时间:5 year
Composite of all-cause mortality or re-hospitalization for worsening heart failure at 5-year follow-up.
5 year
All-cause mortality
大体时间:1 year
All-cause mortality at 1 year
1 year
All-cause mortality
大体时间:2 year
All-cause mortality at 2 year
2 year
All-cause mortality
大体时间:3 year
All-cause mortality at 3 year
3 year
All-cause mortality
大体时间:4 year
All-cause mortality at 4 year
4 year
All-cause mortality
大体时间:5 year
All-cause mortality at 5 year
5 year
Heart failure re-hospitalization
大体时间:1 year
Heart failure re-hospitalization at 1 year
1 year
Heart failure re-hospitalization
大体时间:2 year
Heart failure re-hospitalization at 2 year
2 year
Heart failure re-hospitalization
大体时间:3 year
Heart failure re-hospitalization at 3 year
3 year
Heart failure re-hospitalization
大体时间:4 year
Heart failure re-hospitalization at 4 year
4 year
Heart failure re-hospitalization
大体时间:5 year
Heart failure re-hospitalization at 5 year
5 year
Cardiovascular mortality
大体时间:1 year
Cardiovascular mortality at 1 year
1 year
Cardiovascular mortality
大体时间:2 year
Cardiovascular mortality at 2 year
2 year
Cardiovascular mortality
大体时间:3 year
Cardiovascular mortality at 3 year
3 year
Cardiovascular mortality
大体时间:4 year
Cardiovascular mortality at 4 year
4 year
Cardiovascular mortality
大体时间:5 year
Cardiovascular mortality at 5 year
5 year
All-cause mortality or heart failure re-hospitalization
大体时间:1 year
Evaluation of the composite outcome (all-cause mortality or heart failure re-hospitalization) at 1-year follow-up compared with a historical cohort.
1 year
MR severity
大体时间:1 year
MR severity at 1 year
1 year
MR severity
大体时间:2 year
MR severity at 2 year
2 year
MR severity
大体时间:3 year
MR severity at 3 year
3 year
MR severity
大体时间:4 year
MR severity at 4 year
4 year
MR severity
大体时间:5 year
MR severity at 5 year
5 year
TR severity
大体时间:1 year
TR severity at 1 year
1 year
TR severity
大体时间:2 year
TR severity at 2 year
2 year
TR severity
大体时间:3 year
TR severity at 3 year
3 year
TR severity
大体时间:4 year
TR severity at 4 year
4 year
TR severity
大体时间:5 year
TR severity at 5 year
5 year
LVEF
大体时间:1 year
LVEF at 1 year
1 year
LVEF
大体时间:2 year
LVEF at 2 year
2 year
LVEF
大体时间:3 year
LVEF at 3 year
3 year
LVEF
大体时间:4 year
LVEF at 4 year
4 year
LVEF
大体时间:5 year
LVEF at 5 year
5 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Josep Rodes Cabau, MD PhD、IUCPQ-UL

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月5日

初级完成 (估计的)

2029年6月5日

研究完成 (估计的)

2034年6月5日

研究注册日期

首次提交

2026年5月28日

首先提交符合 QC 标准的

2026年5月28日

首次发布 (实际的)

2026年6月3日

研究记录更新

最后更新发布 (实际的)

2026年6月3日

上次提交的符合 QC 标准的更新

2026年5月28日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data (IPD) will not be publicly shared due to patient confidentiality and privacy considerations, as well as institutional and ethical restrictions governing the use of clinical research data.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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