Prospective, Multicenter, Parallel-Controlled Clinical Study on the Use of Huaier Granules for the Treatment of Bevacizumab- and Anlotinib-Related Proteinuria in Lung Cancer Patients
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 40
研究概览
简要总结
This study is a prospective, multicenter, parallel-controlled clinical trial designed to evaluate the therapeutic efficacy of Huaier Granules for proteinuria occurring in lung cancer patients undergoing treatment with either Bevacizumab or Anlotinib.
详细描述
This study is a prospective, multicenter, parallel-controlled exploratory trial. It plans to enroll 40 subjects diagnosed with malignant lung tumors, who will visit the selected research centers from October 2025 to October 2026. All subjects will be assigned to either the control group or the experimental group based on clinical management and their own preference. Subjects in the control group will receive no therapeutic intervention, while those in the experimental group will be administered Huaier Granules.Throughout the study period, the planned duration for subject recruitment and enrollment is 12 months. The total follow-up duration for enrolled subjects is 48 weeks. After enrollment, subjects will be followed up every 2 weeks during the first 8 weeks, and then every 4 weeks thereafter. Follow-ups will continue until the study ends, the subject withdraws from the study for any reason, is lost to follow-up, or dies, whichever occurs first.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥18 years;
- •Histopathologically confirmed diagnosis of lung cancer;
- •Receiving Bevacizumab or Anlotinib treatment;
- •Positive urine protein detection, with 0.15g < 24-hour urinary protein quantification < 3.5g;
- •No treatment with Huaier Granules within one month prior to enrollment;
- •Expected survival time not less than 6 months;
- •Voluntary participation in this study and provision of signed informed consent.
排除标准
- •Known allergy, contraindication, or caution to any component of Huaier Granules;
- •Inability to take oral medication;
- •Required or ongoing use of drugs known to potentially affect proteinuria, including but not limited to ACE inhibitors, glucocorticoids (>3 weeks), and Chinese patent medicines (as per respective drug prescribing information);
- •Proteinuria caused by underlying diseases, including but not limited to nephropathy, hypertension, urinary tract infection, systemic lupus erythematosus, multiple myeloma, etc.;
- •Women who are pregnant, breastfeeding, or planning pregnancy;
- •Currently participating in other clinical trials investigating drugs for treating proteinuria;
- •Refusal to cooperate with follow-up;
- •Any other reasons deemed by the investigator as unsuitable for participation in this study.