CTRI/2020/06/025595招募中未知
Philips Magnetic Resonance Study Protocol — Human Volunteer Scanning for System Feasibility, Optimization, Demonstration and Education
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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