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临床试验/ITMCTR2000004184
ITMCTR2000004184招募中1 期

Clinical effects of Xingxiao Pill in the treatment of cancer

Dongfang Hospital, Beijing University of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

性别
All

入选标准

  • 1) Patients will be diagnosed as malignant tumors with cytological or histopathological diagnosis , including respiratory tract tumors, gastrointestinal tumors and reproductive system tumors;
  • 2) Patients who have received chemotherapy in the past 1 month;
  • 3) Aged >= 18 years;
  • 4) Eastern Cooperative Oncology Group (ECOG) score <= 2 and estimated survival time > 1 month;
  • 5) Have certain reading ability;
  • 6) Voluntarily agree to participate in this study and sign the informed consent.

排除标准

  • 1) Hyperthermia occurs within two weeks with a body temperature of more than 38 degrees C, or there is obvious active infection;
  • 2) Significant cardiovascular abnormalities (e.g., myocardial infarction, superior vena cava syndrome, grade 2 or above heart disease or uncontrolled hypertension before enrollment (systolic blood pressure over 160 mmHg or diastolic blood pressure over 100mmHg);
  • 3) Serum bilirubin is 1.5 times higher than the upper limit of the reference range of normal value;
  • 4) The serum myoliver is 1.5 times higher than the upper limit of the reference range of normal value or myoliver clearance rate < 50 ml/min;
  • 5) ALT or AST > in the absence of liver metastasis; 2.5 times the upper limit of the normal value, or 5 times the upper limit of the reference range of ALT or AST in the case of liver metastasis;
  • 6) Pregnant or lactating women;
  • 7) Persons with mental illness or intellectual or language impairment;
  • 8) Patients who are known to be allergic to the components used in the study;
  • 9) Patients who are participating in other drug trials within the past month or so;

研究者

发起方
Dongfang Hospital, Beijing University of Chinese Medicine

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