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临床试验/JPRN-jRCTs041190064
JPRN-jRCTs041190064招募中1 期

Thei intraoperative fluorecescene fluore by means of the indocyanine green and near infrated optical imaging

MUTO Jun0 个研究点目标入组 300 人开始时间: 2019年9月2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
300

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
>= 18age old 至 <= 75age old(—)
性别
All

入选标准

  • The following patients WILL BE included in the study
  • 1.Those who are diagnosed to have brain or spinal tumor by CT scan or MRI
  • 2. Those who do not possess any serious hematological and renal conditions, physical examination findings, and past medical history including familial history
  • 3.Those who are be able to sign a written informed consent. However, if incapacitated, a legal surrogate may consent on his/her behalf
  • 4. Those who are younger 18 years and older 75 years of age, regardless of gender; and
  • 5. Those who will undergo surgical treatment.

排除标准

  • The following patients WILL BE excluded FROM the study
  • 1. Those who have an allergy for iodine
  • 2. Those who have a creatine clearance of lower 30 mL .min (Cockroft-Gault)
  • 3. Those who are taking biguanides for diabetes mellitus
  • 4. Those who have dementia or any psychiatric disease
  • 5. Those who have a concomitant hepatic dysfunction, Gamma GTP more than 100, proton-beam time less than 60%, bilirubin more than 51 micro mol. L
  • 6. Those who are pregnant
  • 7. Those who are receiving hemodialysis treatment
  • 8.Those who do not consent, may remove this part since it was already mentioned in the inclusion
  • 9. Those who will be undergoing further examinations, other than the present study, necessitating iodine contrast, to avoid potential toxicity
  • 10. And those who are deemed not appropriate for the study as evaluated by the any of the investigators.

研究者

发起方
MUTO Jun

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