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临床试验/NCT07069673
NCT07069673招募中不适用

Abbott Cephea Mitral Valve Disease Registry

Abbott Medical Devices32 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2025年8月13日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,000
试验地点
32
主要终点
Primary Objective

研究概览

简要总结

The objective of this registry is to gather clinical data on symptomatic patients with mitral valve disease, including patients with mitral regurgitation, mitral stenosis, and mixed mitral valve disease. Data collected from this registry are expected to improve our understanding of the impact of correcting symptomatic mitral valve disease on clinical outcomes in patients that could be candidates for Transcatheter Mitral Valve Replacement and may also inform future regulatory or reimbursement submission strategies for the Cephea Mitral Valve System.

研究设计

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

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

  • Symptomatic mitral valve disease resulting in mitral regurgitation and/or severe mitral valve stenosis.
  • New York Heart Association (NYHA) Functional Class II, III, or ambulatory IV.
  • In the judgement of the Site Heart Team, transcatheter therapy is deemed to be more appropriate than conventional mitral valve surgery, TMVR is more likely to provide an optimal result than TEER, and the subject has been adequately treated per applicable standards, including for coronary artery disease, left ventricular dysfunction, and heart failure.
  • Age 18 years or older at time of consent.
  • The subject agrees to the study requirements, permits all follow-up data entry, and has provided written informed consent.

排除标准

  • Prior surgical or interventional treatment that interferes with the Cephea valve delivery or function.
  • Subject is undergoing dialysis or experiencing chronic renal failure
  • Subject has chronic lung disease requiring continuous home oxygen therapy or chronic outpatient oral steroid use
  • Subjects with comorbidities that are likely to result in a life expectancy of less than 12 months.
  • Pregnant or nursing subjects and those who plan pregnancy during the follow-up period.

研究组 & 干预措施

Potential transcatheter mitral valve replacement (TMVR) candidates

Patients with symptomatic mitral valve disease who may be candidates for transcatheter mitral valve replacement.

结局指标

主要结局

Primary Objective

时间窗: From enrollment to 2 years of follow-up

The objective of the MVD Registry is to collect data on the progression of MVD patients considered for TMVR therapy to guide product development, regulatory submissions, and reimbursement planning

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (32)

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