IRCT20180722040556N8尚未招募3 期
Curcumin in the prevention of cisplatin-induced acute nephrotoxicity: a randomized,double-blind, placebo-controlled ?clinical trial
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
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