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临床试验/NL-OMON35018
NL-OMON35018已完成不适用

Effects of Cimetidine on Cisplatin-induced Nephrotoxicity - 'Effects of Cimetidine on Cisplatin-induced Nephrotoxicity'

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20

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

  • Histological or cytological confirmed diagnosis of any form of irresectable Head and Neck cancer, which is not currently being treated with cisplatin;
  • Treatment with high doses of cisplatin (3-weekly 100 mg/m2), with radiotherapy. No other systemic anti-cancer treatment is allowed.
  • Age =/>18 years;
  • WHO performance =/<1
  • Adequate hematological functions (ANC > 1.5 x 109/L, platelets > 100 x 1012/L)
  • Adequate renal and hepatic functions (serum creatinin < 1.25xULN, bilirubin < 1.25xULN, ALAT and ASAT < 2.5xULN, in case of liver metastasis < 5 ULN; alkaline phosphatase < 5xULN);
  • Written informed consent;
  • Complete initial work-up within four weeks prior to therapy with cisplatin or the combination of cisplatin and cimetidine.

排除标准

  • Pregnant or lactating patients; patients with reproductive potential must use a reliable method of contraception (excluding oral contraceptives), if required;
  • Serious illness or medical unstable condition requiring treatment, symptomatic CNS-metastases or history of psychiatric disorder that would prohibit the understanding and giving of informed consent;
  • Current use of cisplatin therapy;
  • Patients with Chronic Kidney Disease;
  • Major surgery within 4 weeks before start of the protocol (to be evaluated by an MD);
  • (Chronic) use of CYP3A and/or ABCB1/ABCG2 inhibiting and inducing medication, dietary supplements, or other inhibiting compounds (see Appendix D);
  • Unwillingness to change medication, or no adequate alternatives available, when drugs are taken that are known to interact with CYP3A and/or ABCB1 and/or ABCG2;
  • Use of cimetidine 4 weeks prior to study entry.

研究者

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