跳至主要内容
临床试验/NL-OMON52161
NL-OMON52161招募中2 期

Selective Indocyanine Green Injection of a Segmental Hepatic Artery Followed by Near-Infrared Fluorescence Guided Anatomical Liver Resection: A Feasibility Study - SELECT Study

eids Universitair Medisch Centrum0 个研究点目标入组 12 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
12

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
18 至 99(—)

入选标准

  • 1. Scheduled for open or laparoscopic anatomical liver resection;
  • 2. Patients aged over 18 years old;
  • 3. Has the ability to communicate well with the investigator in Dutch or
  • English and willing to comply with the study design;
  • 4. Signed informed consent prior to any study-mandated procedure.

排除标准

  • 1. Previous major abdominal surgery 2. Known allergy or history of adverse reaction to ICG, lipiodol, gel foam, iodine or iodine contrast agents; 3. Child Pugh B or C 4. Portal hypertension or portal vein thrombosis 5. eGFR: <30; in case of eGFR 30-59 metformin should be stopped >48 hours prior to Lipiodol administration and continued >48 hours after Lipiodol administration 6. Hyperthyroidism or a benign thyroid tumor; 7. Pregnant or breastfeeding women; 8. Scheduled for palliative surgery or terminally ill 9. Any condition that the investigator considers to be potentially jeopardizing the patient*s well-being or the study objectives (following a detailed medical history and physical examination); 10. Subject taking phenobarbital, phenylbutazone, primidone, phenytoin, haloperidol, nitrofurantoin, and/or probenecid; 11. Emergency surgery.

研究者

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