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临床试验/NCT02942667
NCT02942667已完成不适用

Magnetic Resonance Imaging of Human Biometrics

Medtronic Cardiac Rhythm and Heart Failure0 个研究点目标入组 12 人开始时间: 2016年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
12
主要终点
Collect High Quality MRI Data

研究概览

简要总结

The primary objective is to collect high quality MRI data (un-processed or processed) from participating subjects for Medtronic research purposes.

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

  • Subject is at least 18 years of age
  • Subject is willing and able to undergo study requirements

排除标准

  • Subject has a medical condition that precludes the subject from participation
  • Subject has any magnetizable foreign object (e.g. jewelry) which cannot be removed for the duration of the study
  • Subject is claustrophobic
  • Subject is unable to stand without assistance
  • Subject requires sedation for MRI scans
  • Subject is implanted with non-Magnetic Resonance conditional or other medical device:
  • Non-MRI conditional pacemaker, Implantable Cardiac Defibrillator (ICD), Cardiac Resynchronization Therapy (CRT), or an implantable hemodynamic monitor
  • Metal clips (i.e. brain aneurysm clip)
  • Artificial heart valve
  • Implanted neural stimulator
  • Gastric capsule camera
  • Swan Ganz catheter
  • Inferior Vena Cava (IVC) filter
  • Orthopedic implant
  • Eye prosthesis
  • Vascular access port
  • Penile prosthesis
  • Intrauterine device
  • Subject has a cochlear implant, middle ear prosthesis, or has had ear surgery
  • Subject has ocular foreign bodies (i.e. metal shavings)
  • Subject has any type of device held in place by a magnet (i.e. dentures)
  • Subject has an insulin pump
  • Subject has metal shrapnel
  • Subject is pregnant or lactating
  • Subject has magnetizable implant
  • Subject requires legally authorized representative to sign Patient Informed Consent (PIC)/ Informed Consent (IC) form
  • Subject has other contraindication for an MRI scan as defined by the study site

结局指标

主要结局

Collect High Quality MRI Data

时间窗: Approximately 6 Weeks

次要结局

未报告次要终点

研究者

发起方
Medtronic Cardiac Rhythm and Heart Failure
申办方类型
Industry
责任方
Sponsor

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