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临床试验/ITMCTR2100005242
ITMCTR2100005242招募中1 期

Clinical observation of auxiliary function of anti-inflammatory Chinese herbal medicine in chemotherapy of middle and advanced lung cancer

Hubei Cancer Hospital0 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 —(—)
性别
All

入选标准

  • 1. The patients voluntarily joined the study, signed the informed consent form, and had good compliance.
  • 2. Patients diagnosed with lung cancer according to imaging, cytology and histological examinations; patients diagnosed with lung cancer in stages IIIB-IV according to the 8th edition of the International Union Against Cancer (UICC) revised TNM staging.
  • 3. Patients who are or will be receiving platinum-based chemotherapy.
  • 4. Estimated survival > 3 months.
  • 5. KPS score > 60 points.
  • 6. Aged >= 18 years.

排除标准

  • 1. Those with other active malignant tumors or those who have not recovered from other major operations before;
  • 2. There are factors that obviously affect the absorption of oral drugs, such as inability to swallow, chronic diarrhea and intestinal obstruction;
  • 3. Complicated with severe infection or confirmed to have other major physiological dysfunction;
  • 4. Patients with serious diseases such as the heart, liver, kidney, hematopoietic system, as well as those with severe functional impairment, and mentally ill patients;
  • 5. Pregnant and lactating patients;
  • 6. Those who cannot cooperate with the treatment;
  • 7. Allergic constitution, history of allergy to chrysanthemum, licorice, or history of severe food or drug allergy.

研究者

发起方
Hubei Cancer Hospital

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