跳至主要内容
临床试验/NL-OMON54396
NL-OMON54396招募中不适用

Prospective use of Philips *iSuite* electroanatomical mapping system in addition to standard CMR-guided electrophysiological procedures. - Use of iSuite during CMR-guided electrophysiological procedures.

Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • •- Already scheduled by the treating electrophysiologist for CMR-EP as standard
  • •care for the treatment of a cardiac arrhythmia.
  • •- Minimum age of 18 years old.
  • •- Written informed consent.

排除标准

  • •- Participation in another investigational study that has not reached its
  • •primary endpoint.
  • •- Refusal of data storage until 15 years after end of study.
  • •To be noted: All patients that are included in this study are already scheduled
  • •and thus considered eligible for CMR-EP by the treating electrophysiologist. A
  • •strict prerequisite for CMR-EP is that the patient has no contraindication for
  • •MRI (metallic implant, body weight > 130 kg, pregnancy, breast feeding women,
  • •known severe allergy to gadolineum contrast agents, renal failure with eGFR <=
  • •30 mL/min/1,73m2) or contraindication for an EP procedure.

研究者

发起方
Medisch Universitair Ziekenhuis Maastricht

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