The Asia-Pacific Mitral & Tricuspid Valve-in-Valve/Valve-in-Ring Registry (AP ViV Registry)

National Heart Centre Singapore8 个研究点分布在 6 个国家目标入组 150 人开始时间: 2025年3月17日最近更新: 2025年7月10日

试验速览

阶段: 不适用
状态: 招募中
发起方: National Heart Centre Singapore
入组人数: 150
试验地点: 8
主要终点: All-cause mortality

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

A retrospective and prospective, observational, multicenter cohort study of consecutive patients undergoing transcatheter mitral/tricuspid ViV or ViR procedure with balloon expandable valve across participating sites in Asia-Pacific.

研究设计

研究类型: Observational
观察模型: Case Only
时间视角: Other

入排标准

年龄范围: 21 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Had at least one documented Mitral valve-in-valve/valve-in-ring procedure done during the period of 1 Jan 2023 to current date. (Retrospective) OR Planned to undergo a Mitral valve-in-valve/valve-in-ring procedure. (Prospective) OR Had at least one documented Tricuspid valve-in-valve/valve-in-ring procedure done during the period of 1 Jan 2023 to current date. (Retrospective) OR Planned to undergo a Tricuspid valve-in-valve/valve-in-ring procedure. (Prospective)

排除标准

•Active endocarditis
•Any other conditions which investigator deems unsuitable for participation.

结局指标

主要结局

All-cause mortality

时间窗: From date of procedure to 10 years

次要结局

未报告次要终点

研究者

发起方

National Heart Centre Singapore

申办方类型

Other

责任方

Sponsor

研究点 (8)

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