ITMCTR2100004896招募中1 期
A randomized, double-blind, placebo-controlled trial of Qidong Bufei Decoction in treating postoperative symptoms of non-small cell lung cancer
适应症
试验速览
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 75（—）
- 性别
- All
入选标准
- •1. Postoperative patients with stage I non-small cell lung cancer diagnosed by pathology or cytology;
- •2. Enroll in the group within two weeks after thoracoscopy;
- •3. Aged 18-75 years;
- •4. Physical condition score ECOG 0-2 points;
- •5. Estimated survival period >= 6 months;
- •6. Neutrophils>1.5x10^9/L, platelets > 100x10^9/L, hemoglobin>9.0g/dl; normal bilirubin or < 1.5xULN; AST (SGOT), ALT (SGPT)< 2.5xULN; serum creatinine < 1.5xULN.
排除标准
- •1. Patients who received neoadjuvant chemotherapy before surgery;
- •2. Those who intend to receive radiotherapy, chemotherapy, targeted drug therapy and other treatment methods within 1 month after surgery;
- •3. Patients with severe complications such as pulmonary embolism, respiratory failure, and myocardial infarction during the perioperative period;
- •4. In other clinical trials;
- •5. Patients during pregnancy or lactation;
- •6. Patients with a history of mental illness that is difficult to control;
- •7. Those who are allergic to study drugs;
- •8. Those who cannot understand and refuse to sign the informed consent form;
- •9. Those who cannot cooperate with the scale data collector.
研究者
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