跳至主要内容
临床试验/IRCT20180722040556N8
IRCT20180722040556N8尚未招募3 期

Curcumin in the prevention of cisplatin-induced acute nephrotoxicity: a randomized,double-blind, placebo-controlled ?clinical trial

Esfahan University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
100

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 years 至 no limit(—)
性别
All

入选标准

  • Creatinine Clearance higher than 45 mL/min based on CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration)
  • The patient who will have enough compliance and ability to take curcumin orally.
  • All adult cancer 's patients who will receive a regimen contains cisplatin (with the usual recommended dose between 50-100 mg / m2 )

排除标准

  • Patients with active infection or symptoms of sepsis.
  • Patients who have received nephrotoxic drugs such as aminoglycoside, amphotericin, vancomycin, colistin, media contrast, calcineurin inhibitors or Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) for the past 72 hours.
  • Patients who are taking ifosfamide in their chemotherapy regimen
  • Patients who are taking fluvoxamine, anagrelide, or hydroxy progesterone in their treatment regimen.
  • Patients who may experience complications or allergic reactions to curcumin during treatment.
  • Patients who had a history of acute kidney injury ( AKI ) before entering the study.
  • Patients with bilirubin above 2 mg / dl or liver enzymes above 2.5 times the normal level.

研究者

相似试验