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临床试验/TCTR20170621002
TCTR20170621002尚未招募2 期

Efficacy and Safety of Thai Herbal Formularies Benja Amarit in Hepatocellular Carcinoma Patients: Clinical Trial Phase II

Department of Thai Traditional and Alternative Medicine0 个研究点目标入组 81 人开始时间: 2017年6月21日最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
入组人数
81

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • 1. Patients who have been diagnosed is Hepatocellular carcinoma Child-Pugh score class A OR B.
  • 2. Patients who cannot treat by standard treatment.
  • 3. Stop another treatment not less than 4 weeks.
  • 4. Stop radiation and chemotherapy not less than 4 weeks.
  • 5. Thai, age between 18-80 years.
  • 6. Zubrod-ECOG-WHO score between 0-2.
  • 7. Patients who was evaluated to survival more than 5 months.
  • - To understand Thai language and to communicate with research assistants to assess side effects from treatment
  • - Can receive medication and follow up as prescribed
  • - Consent and sign the name in research

排除标准

  • 1. Patients who have been allergy to ingredient of formularies Benja Amarit
  • 2. Pregnant or breastfeeding women.
  • 3. Receive chemotherapy or use herb or vitamin, its out of standard treatment.
  • 4. Patient who have acute illness such as sepsis.

研究者

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