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临床试验/ISRCTN11165621
ISRCTN11165621已完成未知

Feasibility of ultrasound as a temporary pacing or resynchronization technique, an acute clinical evaluation

Medtronic, Inc.0 个研究点目标入组 20 人开始时间: 2019年3月8日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Meets standard criteria for implantation of a CRT-P or CRT-D device according to local guidelines
  • 2. Subject (or legally authorized representative) has signed and dated the Informed Consent Form
  • 3. Aged 18 years or older

排除标准

  • 1. Confirmed myocardial damage, cardiac or chest surgery, or coronary procedure within the previous 30 days
  • 2. Enrolled in a concurrent study that may confound the results of this study, without documented pre-approval from a Medtronic study manager
  • 3. Pregnant, or of childbearing potential and not on a reliable form of birth control. Women of childbearing potential are required to have a negative pregnancy test within 7 days prior to the PACE-US Procedure visit.
  • 4. Meets exclusion criteria required by local law (e.g. age, etc.)
  • 5. Has any medical condition that would limit study participation per physician discretion

研究者

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