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
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