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PRECISE-AFMR I: Transcatheter Mitral Valve Edge-to-Edge Repair for Atrial Functional Mitral Regurgitation in Patients at High Surgical Risk (PRECISE-AFMR I)

PRECISE-AFMR I: A Prospective Randomized Controlled Trial of Transcatheter Mitral Valve Edge-to-Edge Repair in Patients With Atrial Functional Mitral Regurgitation at High Surgical Risk

Atrial functional mitral regurgitation (AFMR) develops when enlargement and remodeling of the left atrium and mitral annulus prevent the mitral valve leaflets from closing completely, allowing blood to leak backward through the valve. For patients with significant AFMR who remain symptomatic despite medical treatment and are at high risk for surgery, it is uncertain whether adding transcatheter mitral valve edge-to-edge repair (TEER), a catheter-based procedure that brings the mitral valve leaflets together, provides better outcomes than medical treatment alone.

PRECISE-AFMR I is a prospective, multicenter, randomized study that will enroll 182 adults with moderate-to-severe or severe AFMR, high or prohibitive surgical risk, and mitral valve anatomy suitable for TEER. Participants will be assigned in a 1:1 ratio to receive TEER plus optimized guideline-directed medical therapy (GDMT) or optimized GDMT alone. All participants will receive standardized medical care and will be followed for 12 months.

The main effectiveness outcome is the occurrence of death from any cause or hospitalization for heart failure within 12 months. The main safety outcome is the occurrence of major device-related adverse events within 12 months. The study will also assess mitral regurgitation severity, symptoms, functional capacity, quality of life, heart failure events, and use of health care resources.

研究概览

详细说明

PRECISE-AFMR I is designed to address the limited randomized evidence for transcatheter edge-to-edge repair (TEER) in patients with atrial functional mitral regurgitation (AFMR). The study uses standardized phenotypic and imaging assessment to identify patients in whom AFMR is the predominant mechanism of mitral regurgitation and whose mitral valve anatomy is considered suitable for TEER.

Before randomization, each participant will provide written informed consent and undergo clinical, laboratory, and imaging assessments. Echocardiographic data will be submitted to an independent echocardiography core laboratory (ECL) for confirmation of the AFMR diagnosis, mitral regurgitation severity, left ventricular function, left atrial remodeling, and anatomical suitability for TEER. An eligibility committee will then review the clinical findings, surgical risk, prior treatment, and ECL assessment. Only participants confirmed as eligible by both the ECL and the eligibility committee will proceed to randomization.

Eligible participants will be randomly assigned in a 1:1 ratio to TEER plus optimized guideline-directed medical therapy (GDMT) or optimized GDMT alone. Randomization will be performed through a central randomization system or electronic data capture system using blocked randomization stratified by study center or center group. The allocation sequence will be generated and maintained independently, and treatment assignment will not be released until eligibility and baseline assessments have been completed.

Because TEER is an interventional procedure, participants and treating investigators will not be blinded to treatment assignment. To reduce potential assessment bias, key echocardiographic measurements will be centrally reviewed by the ECL, and major clinical and safety events will be adjudicated by an independent clinical events committee that is blinded to treatment assignment whenever feasible. Both groups will receive comparable follow-up intensity, event collection, heart failure management, atrial fibrillation management, anticoagulation or antiplatelet therapy when clinically indicated, and management of comorbid conditions.

Participants assigned to the TEER group will undergo the procedure in addition to continued optimized GDMT and standardized clinical care. TEER is intended to be performed as soon as clinically feasible after randomization, preferably within 14 days and, when medically delayed, within 30 days whenever possible. Participants assigned to the control group will not undergo planned TEER before completion of the 12-month primary evaluation period and will receive individualized optimization of GDMT and other indicated standard treatments.

All randomized participants will be followed for 12 months, with major assessments conducted at baseline, treatment or discharge, 30 days, 6 months, and 12 months. Rescue TEER or another necessary intervention may be considered for participants in the GDMT group who experience clinically significant deterioration despite optimized treatment. Such treatment will require reassessment by the heart team, confirmation that the anticipated benefit outweighs the risk, and renewed informed consent. Rescue treatment and crossover events will be fully documented, while the primary efficacy analysis will follow the intention-to-treat principle.

Study data will be collected using standardized case report forms or an electronic data capture system. The ECL will centrally review key imaging outcomes, the clinical events committee will adjudicate major clinical and safety events, and an independent data and safety monitoring board will periodically review participant safety and study conduct.

研究类型

介入性

注册 (估计的)

182

阶段

  • 不适用

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

学习地点

      • Beijing、中国
        • Fuwai Hospital
        • 接触:

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

描述

Inclusion Criteria:

  • 1. Aged ≥18 years;

    2. Presence of symptoms of heart failure, with New York Heart Association (NYHA) functional class II, III, or ambulatory class IV;

    3. Confirmed by preliminary assessment of the study-site Heart Team and review by the Echocardiography Core Laboratory (ECL) to have at least moderate-to-severe atrial functional mitral regurgitation (AFMR), generally graded as 3+ or 4+;

    4. At least one hospitalization for heart failure within the 12 months prior to enrollment and/or a plasma B-type natriuretic peptide (BNP) level ≥300 pg/mL or N-terminal pro-B-type natriuretic peptide (NT-proBNP) level ≥1,500 pg/mL;

    5. As confirmed by a heart failure specialist at the study site, the subject has received maximally optimized guideline-directed medical therapy (GDMT) and other necessary standardized comprehensive treatment in accordance with current guidelines for at least 3 months. For subjects with concomitant atrial fibrillation, coronary artery disease, or other potentially correctable comorbidities, appropriate evaluation and guideline-recommended management must have been completed, or the subject must have been clearly determined to be unsuitable for further treatment;

    6. Determined by the multidisciplinary Heart Team, in accordance with the process described in Section 4.7, to be at high surgical risk, to have a contraindication to surgery, or to be unsuitable for surgery, or determined after comprehensive assessment that surgical treatment is not the optimal current strategy;

    7. During the screening period or within 90 days prior to randomization, mitral valve anatomy is assessed by echocardiography at the study site and confirmed by the ECL to be suitable for transcatheter edge-to-edge repair (TEER). Anatomical suitability must meet at least all of the following criteria:

    • Mitral valve area >4.0 cm² and baseline mean transmitral pressure gradient <4 mmHg;

      • Adequate mobility or sufficient graspable leaflet tissue in the target grasping area, with a mobile/graspable leaflet length ≥10 mm;

        • Mitral annular anteroposterior diameter ≤40 mm;

          • Left atrial volume index (LAVI) <85 mL/m²;

            ⑤ Leaflet-to-annulus index (LAI) >1.10;

            8. The transseptal puncture route and femoral venous access are considered suitable for TEER by the investigator or Heart Team;

            9. The subject or the subject's legally authorized representative voluntarily agrees to comply with the requirements of the study protocol, including the possibility of being randomized to the optimized GDMT group, and provides written informed consent.

Exclusion Criteria:

  • 1. Presence of primary structural mitral valve disease that can independently account for the mitral regurgitation (MR), such as leaflet prolapse, flail leaflet, rheumatic valvular disease, leaflet perforation, or damage resulting from infective endocarditis;

    2. Functional mitral regurgitation other than atrial functional mitral regurgitation (AFMR), including ventricular functional mitral regurgitation caused by left ventricular dilatation, regional wall-motion abnormalities, ischemic cardiomyopathy, dilated cardiomyopathy, or other conditions involving the myocardium, including restrictive cardiomyopathy, hypertrophic cardiomyopathy, and infiltrative cardiomyopathy such as amyloidosis, hemochromatosis, or sarcoidosis;

    3. Presence of pericardial disease, such as constrictive pericarditis, that may be the predominant mechanism underlying heart failure or MR;

    4. Prior surgical mitral valve intervention or transcatheter mitral valve intervention;

    5. Concomitant moderate-to-severe or greater disease of another heart valve requiring surgical or transcatheter intervention;

    6. An acute cerebrovascular event within the previous 30 days;

    7. Cardiovascular or cerebrovascular surgery or interventional treatment within the previous 30 days, including coronary artery bypass grafting (CABG), percutaneous coronary intervention (PCI), transcatheter aortic valve replacement (TAVR), or transcatheter carotid artery stenting;

    8. Severe symptomatic carotid artery stenosis, defined as >70% stenosis on ultrasonography;

    9. Hemodynamic instability requiring continuous intravenous drug infusion or mechanical circulatory support;

    10. Pulmonary artery systolic pressure (PASP) >70 mmHg as estimated by echocardiography, or pulmonary vascular resistance (PVR) >3 Wood units as measured by right heart catheterization;

    11. Symptoms, signs, or echocardiographic evidence of severe right ventricular dysfunction, such as tricuspid annular plane systolic excursion (TAPSE) <15 mm or peak systolic tissue Doppler velocity (S') <10 cm/s;

    12. Chronic renal insufficiency requiring long-term hemodialysis;

    13. Severe liver cirrhosis accompanied by esophageal varices;

    14. Prior heart transplantation;

    15. Severe chronic obstructive pulmonary disease (COPD) requiring continuous home oxygen therapy or long-term oral glucocorticoid therapy;

    16. Severe hematologic disease;

    17. A modified Rankin Scale score ≥4, indicating moderately severe or severe disability;

    18. Mitral valve anatomical features that, as assessed by echocardiography at the study site and confirmed by the Echocardiography Core Laboratory (ECL), may prevent safe implantation, appropriate positioning, stable leaflet grasping, or adequate reduction of MR with the transcatheter edge-to-edge repair (TEER) device. Such features include, but are not limited to, insufficient leaflet mobility or insufficient graspable leaflet tissue in the target grasping area, significant calcification in the grasping area, a prominent leaflet cleft, leaflet perforation, severe leaflet thickening, fibrosis, retraction, or severely restricted leaflet mobility, insufficient primary or secondary chordal support, or any other anatomical feature that, in the judgment of the ECL, may result in technical failure of TEER, significant residual MR, or an increased risk of clinically significant mitral stenosis after the procedure;

    19. An intracardiac mass, thrombus, or vegetation detected by echocardiography;

    20. A contraindication to, or a high risk associated with, transesophageal echocardiography;

    21. Inadequate echocardiographic image quality;

    22. Known allergy or contraindication to any medication or device material required for the TEER procedure;

    23. Pregnancy, breastfeeding, or intention to become pregnant within the following 12 months;

    24. Anticipated need for emergency surgery or elective cardiac surgery for any reason within the following 12 months;

    25. Life expectancy of <12 months due to a noncardiac condition;

    26. The subject is a member of a vulnerable population or has a condition that may impair their ability to provide written informed consent and/or comply with study procedures;

    27. Current participation in another interventional drug or device trial that may interfere with the assessment of the primary endpoint of this study;

    28. Any other condition that, in the judgment of the investigator, ECL, or EC, renders the subject unsuitable for participation in this study.

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

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:TEER plus optimized GDMT group
Transcatheter edge-to-edge repair (TEER) reduces mitral regurgitation by approximating the anterior and posterior mitral leaflets, increasing the leaflet coaptation area, and reducing the regurgitant orifice area.
无干预:Optimized GDMT group

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
Composite endpoint of all-cause mortality or hospitalization for heart failure within 12 months after randomization.
大体时间:Within 12 months after randomization.
Within 12 months after randomization.
Composite endpoint of device-related major adverse events.
大体时间:Within 12 months after randomization.
  • Single leaflet device attachment (SLDA);
  • Device migration, device embolization, device detachment, or device fracture;
  • Device thrombosis;
  • Device-related infective endocarditis;
  • Mitral stenosis requiring surgical treatment or an unplanned repeat intervention;
  • Non-elective cardiac surgery or unplanned repeat mitral valve intervention due to a device-related complication;
  • Left ventricular assist device implantation;
  • Heart transplantation;
  • Other serious device-related complications adjudicated by the Clinical Events Committee (CEC) as device-related major adverse events in accordance with the Mitral Valve Academic Research Consortium (MVARC) criteria.
Within 12 months after randomization.

次要结果测量

结果测量
措施说明
大体时间
Hierarchical composite endpoint of all-cause mortality, hospitalization for heart failure, or urgent emergency department/outpatient intensification of heart failure therapy within 12 months after randomization
大体时间:within 12 months after randomization
within 12 months after randomization
Proportion of patients with MR ≤1+ at 30 days, 6 months, and 12 months
大体时间:30 days, 6 months, and 12 months
30 days, 6 months, and 12 months
Proportion of patients with MR ≤2+
大体时间:30 days, 6 months, and 12 months
30 days, 6 months, and 12 months
Residual MR grade and change from baseline
大体时间:30 days, 6 months, and 12 months
30 days, 6 months, and 12 months
Change in NYHA functional class and proportion of patients in NYHA class I/II
大体时间:30 days, 6 months, and 12 months
30 days, 6 months, and 12 months
Change from baseline in left atrial anteroposterior diameter
大体时间:at 12 months
at 12 months
Change from baseline in left atrial volume index (LAVI)
大体时间:at 12 months
at 12 months
Change from baseline in 6-minute walk distance (6MWD)
大体时间:at 12 months
at 12 months
Change from baseline in Kansas City Cardiomyopathy Questionnaire (KCCQ) score
大体时间:at 12 months
at 12 months
Change from baseline in BNP or NT-proBNP level
大体时间:at 12 months
at 12 months
Number of recurrent hospitalizations for heart failure
大体时间:within 12 months after randomization
within 12 months after randomization
All-cause mortality
大体时间:within 12 months after randomization
within 12 months after randomization
Cardiovascular mortality
大体时间:within 12 months after randomization
within 12 months after randomization
Non-cardiovascular mortality
大体时间:within 12 months after randomization
within 12 months after randomization
First hospitalization for heart failure
大体时间:within 12 months after randomization
within 12 months after randomization
Total number of hospitalizations for heart failure
大体时间:within 12 months after randomization
within 12 months after randomization
Emergency department visits or outpatient events requiring intensification of heart failure therapy
大体时间:within 12 months after randomization
within 12 months after randomization
Composite endpoint of major procedure-related adverse events
大体时间:within 30 days after the TEER procedure

The composite endpoint includes, but is not limited to, any of the following:

All-cause mortality; Stroke, including ischemic stroke and hemorrhagic stroke, or transient ischemic attack; Acute myocardial infarction; Non-elective cardiac surgery due to device- or procedure-related complications; Life-threatening or major bleeding; Major vascular complications; Stage 2 or 3 acute kidney injury, including new initiation of dialysis; Cardiac tamponade or pericardial effusion requiring interventional or surgical treatment; Clinically significant iatrogenic atrial septal defect requiring treatment; Other serious adverse events adjudicated by the Clinical Events Committee (CEC) as major procedure-related adverse events in accordance with the Mitral Valve Academic Research Consortium (MVARC) criteria.

within 30 days after the TEER procedure

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。

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8月1日

初级完成 (估计的)

2027年12月1日

研究完成 (估计的)

2027年12月1日

研究注册日期

首次提交

2026年7月29日

首先提交符合 QC 标准的

2026年7月29日

首次发布 (实际的)

2026年8月3日

研究记录更新

最后更新发布 (实际的)

2026年8月3日

上次提交的符合 QC 标准的更新

2026年7月29日

最后验证

2026年7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)?

未定

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

是的

在美国制造并从美国出口的产品

是的

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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