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临床试验/NL-OMON39088
NL-OMON39088已完成不适用

The influence of time of administration on tamoxifen pharmacokinetics. - Different times of tamoxifen administration.

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 18 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
18

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 breast cancer, for which treatment with tamoxifen is indicated (to be evaluated by the treating physician);
  • -Use of tamoxifen for at least 4 weeks and willing to continue the treatment until the end of the study;
  • -Age > 18 years;
  • -WHO performance <= 1;
  • -Written informed consent;
  • -Adequate renal and hepatic functions (see protocol);
  • -Adequate hematological blood counts (see protocol);
  • -No chemotherapy within the last 4 weeks before start;
  • -No radiotherapy within the last 4 weeks before start.

排除标准

  • -Pregnant or lactating patients;
  • -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;
  • -More than one tamoxifen dose per day (20 or 40 mg);
  • -Non-compliance.

研究者

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