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临床试验/ITMCTR2000003349
ITMCTR2000003349招募中1 期

Clinical study on the prevention of postoperative recurrence and metastasis of colorectal cancer by Zuojin pill combined with adjuvant chemotherapy

Shuguang Hospital affillated with Shanghai University of TCM0 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

年龄范围
18 至 80(—)
性别
All

入选标准

  • 1. Clear cytology and pathology diagnosis of colorectal cancer (TMN stage for III);
  • 2. The TCM syndrome type was consistent with the syndrome of irascibility in stomach and gastrointestinal dampness and heat.
  • 3. Chemotherapy was planned, and there were no other treatment plans such as radiotherapy, interventional therapy, targeting and immunization during the study period.
  • 4. 1 month before the test, no traditional Chinese medicine, proprietary Chinese medicine or traditional Chinese medicine injection was used for the treatment.
  • 5. Urine HCG test is available for both men and women, aged 18-80 years and of childbearing age.
  • 6. Physical condition score: KPS score: 70 or above;
  • 7. The estimated survival time is 6 months or more;
  • 8. The peripheral blood image was normal, and there were no obvious abnormalities in the cardiac, hepatic, renal and electrocardiogram.
  • 9. No cognitive impairment, willing to participate in this study, able to receive relevant treatment and physical and chemical examinations and sign an informed consent.

排除标准

  • 1. Patients with serious diseases such as cardiovascular system, respiratory system, digestive system, urogenital system, blood system and rheumatic immune system, who cannot tolerate treatment;
  • 2. People with mania, depression, anxiety, schizophrenia, active tuberculosis and other serious infectious diseases;
  • 3. Cancer pain, intestinal obstruction, ascites and other serious tumor complications;
  • 4. Patients who had received radiotherapy, interventional therapy, targeted therapy, immunization and other treatments in the past 2 months;
  • 5. Those who had been enrolled in other experimental drugs in the past 2 months;
  • 6. Those who cannot be treated by TCM compound due to allergy or other reasons;
  • 7. The researcher considers it inappropriate to participate in the study.

研究者

发起方
Shuguang Hospital affillated with Shanghai University of TCM

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