跳至主要内容
临床试验/CTRI/2020/06/025595
CTRI/2020/06/025595招募中未知

Philips Magnetic Resonance Study Protocol — Human Volunteer Scanning for System Feasibility, Optimization, Demonstration and Education

Philips India Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中

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

入选标准

  • 1) Volunteeris willing and capable of providing informed consent and physically capable of performing study related activities.
  • 2) Volunteer age between 18 -65 years old including either sex.
  • 3) Volunteer has passed a general medical health check which involves laboratory investigations like CBC, ESR,RBS, Serum Creatinine, HIV, HbsAg, HCV, Urine analysis, ECG and UPT( for child bearing potential female subjects only).

排除标准

  • 1) Volunteers with any known contraindications for MR scanning
  • 2) Volunteers with Pacemakers or other implanted electronic devices which are Non MR Compatible
  • 3) Volunteers with metal implants which are not MR conditional or MR safe
  • 4) Volunteers with small metal components in the body (vascular clips, metal splinters, stents, etc.) which are not MR conditional or MR safe
  • 5) Volunteers with epilepsy
  • 6) Volunteer with known severe cardiac disorders, Cerebrovascular, Respiratory, Hepatic, Renal, or Congenital anomaly or any other conditions as per the Physician opinion
  • 7) Volunteers with uncontrolled hyper tension and diabetic Mellitus
  • 8) Volunteers with dermal medicinal patches
  • 9) Volunteers with mental illness or diseases, known claustrophobia, anxiety or panic disorders
  • 10) Volunteers with Meniere’s disease or any previous history of tinnitis
  • 11) Pregnant women
  • 12) Volunteers with significant chronic illness

研究者

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