跳至主要内容
临床试验/ISRCTN10645335
ISRCTN10645335进行中(未招募)未知

Intravital microscopy in patients with peritoneal carcinomatosis

Mayo Clinic0 个研究点目标入组 30 人开始时间: 2020年11月25日最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
发起方
Mayo Clinic
入组人数
30

研究概览

简要总结

2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33654117/ (added 06/01/2022)

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • 1. Age =18 years of age
  • 2. Have an ECOG Performance Status of =2
  • 3. Have measurable disease in the peritoneum by direct visualization (visible lesion typically >0.5 cm in maximal diameter)
  • 4. Carcinomatosis that meets indications for CRS-HIPEC
  • 5. Subject must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
  • 6. A negative skin-prick test to fluorescein

排除标准

  • 1. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations
  • 2. Renal dysfunction as defined as a GFR <45
  • 3. Liver dysfunction as defined by Child-Pugh score >5, or LFT's 1.5x above the normal range
  • 4. Any known allergy or prior reaction to fluorescein or ICG or a positive skin prick test to fluorescein
  • 5. Pregnant or nursing female subjects, determined preoperatively with a urine pregnancy test
  • 6. Unwilling or unable to follow protocol requirements
  • 7. Any condition which in the Investigators' opinion deems the patient unsuitable (e.g. abnormal EKG)
  • 8. Any condition that excludes CRS-HIPEC as the standard of care for the patient

研究者

发起方
Mayo Clinic

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