ITMCTR1900002303招募中未知
A multi-center prospective randomized controlled study for Jiedu Granule in the treatment of advanced hepatocellular carcinoma
Changhai Hospital of Traditional Chinese Medicine,Navy Military Medical University0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 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 100（—）
- 性别
- All
入选标准
- •1. Male or female aged older than 18 years;
- •2. Histologically diagnosed HCC, OR clinically diagnosed HCC;
- •3. Documented progression with or intolerance to target therapy for advanced HCC and no indication of transarterial chemoembolization and radiotherapy;
- •4. Stage C and D according to the BCLC staging classification;
- •5. More than 1 month from the last TACE or 2 months from the last radiotherapy.
- •6. The estimated survival time is more than 2 months;
- •7. Willing to participate in clinical trials and sign informed consent.
排除标准
- •1. currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment;
- •2. Local treatment including radiotherapy (except palliative radiotherapy), percutaneous ethanol injection, radiofrequency ablation, transarterial embolization, or cryotherapy administered within 4 weeks prior to enrollment;
- •3. Had a solid organ transplant;
- •4. Presence of brain or leptomeningeal metastases;
- •5. Has had esophageal or gastric variceal bleeding within the last 6 months;
- •6. the researchers consider those who were not suitable for inclusion.
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