跳至主要内容
临床试验/NCT07256678
NCT07256678尚未招募不适用

Jewel P-WCD Post-Approval Study (PAS)

Element Science, Inc.0 个研究点目标入组 6,330 人开始时间: 2026年1月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
6,330
主要终点
Percent of VT/VF events successfully detected by the Jewel P-WCD

研究概览

简要总结

The objective of this PAS is to demonstrate the continued safety and clinical effectiveness of the Jewel P-WCD.

详细描述

This study is an observational registry study of the Jewel P-WCD in post-market use

研究设计

研究类型
Observational
观察模型
Other
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

  • N/A - registry will collect data already obtained commercially from patients prescribed the Jewel P-WCD.

排除标准

  • N/A - registry will collect data already obtained through commercial consent from patients prescribed the Jewel P-WCD

结局指标

主要结局

Percent of VT/VF events successfully detected by the Jewel P-WCD

时间窗: From enrollment to the end of treatment at approximately 90 days

次要结局

未报告次要终点

研究者

发起方
Element Science, Inc.
申办方类型
Industry
责任方
Sponsor

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