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临床试验/DRKS00031712
DRKS00031712Enrolling By Invitation不适用

Philips Magnetic Resonance Study – Human Volunteer Scanning for System Pre-Development

Philips GmbH Innovative Technologies0 个研究点目标入组 4,000 人开始时间: 2023年4月20日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
4,000

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 Years 至 75 Years(—)
性别
All

入选标准

  • Participants willing and capable of providing informed consent and physically capable of performing study related activities (i.e., lying still in a MR scanner)
  • Participant is at least 18 years old and not older than 75 years

排除标准

  • Participant with medical history (anamnesis) of severe hypertension, diabetes, cardiovascular and cerebrovascular diseases, COPD (chronic obstructive pulmonary disease) and other severe acute or chronic diseases (e.g., Cancer)
  • Participants with history of severe congenital diseases such as congenital heart disease.
  • Participant with epilepsy
  • Participant with any type of electronic, mechanical, or magnetic implant (Examples: insulin pump, pacemaker, defibrillator, neurostimulator, cochlear implant)
  • Participant with small metal components in the body (vascular clips, metal splinters, stents, filters or catheters)
  • Participants with contraceptive coils, dental braces etc. which are not MR conditional or MR safe
  • Participant with dermal medicinal patches
  • Participant with any piercings and/or any tattoos and/or permanent make-up
  • Participant with Meniere’s disease or Vertigo
  • Claustrophobia, anxiety disorder or panic attacks
  • Female participant who reports to be pregnant or believes she could be pregnant
  • Eye or other injuries by metal splinters
  • Any known contraindications for MR scanning
  • Unless cleared by a physician:
  • oMetal implants such as surgical implants, prostheses, IUDs
  • oTattoos or permanent make-up
  • oOther disease or condition or incidental findings

研究者

发起方
Philips GmbH Innovative Technologies

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