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临床试验/NL-OMON48005
NL-OMON48005已完成不适用

Cerebral Perfusion and Flow Pulsatility in Patients with Aortic Coarctation * a 7 Tesla MRI Study - RESOLUTION study

niversitair Medisch Centrum Utrecht0 个研究点目标入组 50 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
已完成
发起方
入组人数
50

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
12 至 99(—)

入选标准

  • - Subject has been diagnosed with CoA.
  • - Subject has previously undergone surgical treatment or balloon dilatation for
  • - Subject is 12 years or older.
  • - Subject is competent to understand the performed procedures, the potential
  • hazards associated with these procedures, and to provide written informed
  • - Subject is 12 years or older.
  • - Subject is competent to understand the performed procedures, the potential
  • hazards associated with these procedures, and to provide written informed

排除标准

  • - Subject is currently pregnant.
  • - Subject has previously undergone stent implantation for CoA.
  • - Subject has undergone a cardiovascular intervention between the 7T MRI brain
  • and the combined 3T MRI brain and 3T cardiac MRI, which, in the opinion of the
  • investigator, could adversely affect the interpretation of the results.
  • - Subject has a medical condition which, in the opinion of the investigator,
  • could adversely affect the subject*s safety and/or the interpretation of the
  • - Subject with a contraindication for MRI:
  • o Cardiac pacemaker or implanted cardioverter defibrillator not compatible with
  • o Electronic device or implant, such as cochlear implant or insulin pump.
  • o Known claustrophobia.
  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • - Subject has a history of aortic coarctation or other cardiovascular disease.
  • - Subject has a history of neurological disease or intellectual disability.
  • - Subject is currently pregnant.
  • - Subject has a medical condition which, in the opinion of the investigator,
  • could adversely affect the subject*s safety and/or the interpretation of the
  • - Subject with a contraindication for MRI:
  • o Cardiac pacemaker or implanted cardioverter defibrillator not compatible with
  • o Electronic device or implant, such as cochlear implant or insulin pump.
  • o Known claustrophobia.

研究者

发起方
niversitair Medisch Centrum Utrecht

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