跳至主要内容
临床试验/JPRN-jRCTs031230230
JPRN-jRCTs031230230招募中1 期

Age related cerebral perfusion difference and safty in normal adult study by 123 I-IMP SPECT. .

Hirano Shigeki0 个研究点目标入组 40 人开始时间: 2023年7月14日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 85age old(—)
性别
All

入选标准

  • Those who meet all the following conditions are eligible.
  • 1) Age at consent between 20 to 85.
  • 2) Person who are capable of conducting studies within required period.
  • 3) Subjects who have no problem if neuropsychological examination is performed within 3 months before obtaining informed consent
  • 4) Subjects who are age-appropriate and have no problems if a head MRI scan has been performed within 3 months before obtaining informed consent
  • 5) Subjects who have no problem in neuropsychological examination in the screening test after obtaining informed consent
  • 6)Subjects who have age-appropriate brain MRI images and no problems in the screening test after obtaining informed consent
  • 7)Person who are capable of providing written consent

排除标准

  • Those who meet any of the following conditions are not eligible.
  • 1) Those who are pregnant, or possible pregnancy, or breastfeeding.
  • 2) Those with prior neurological or psychiatric disorders which could interfere with cognitive function.
  • 3) Those with severe physical problem (e.g. in liver, kidney, or endocrine system).
  • 4) Those having prior serious head trauma.
  • 5) Those who are unable to perform MRI (i.e. metallic implants, claustrophobia, tatoos).
  • 6) Those who have impared cognitive function.
  • 7) Those who are incapable of completing the study, judged by the physician.

研究者

发起方
Hirano Shigeki

相似试验