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临床试验/NCT01580358
NCT01580358Unknown不适用

Changhua Christian Hospital

Changhua Christian Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2009年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
60
试验地点
1
主要终点
Change from baseline in EORTC QOL-C30 at four weeks

研究概览

简要总结

Using Shen-Mai-San for cancer patients undergoing chemotherapy or radiotherapy could help these people improve the quality of life.

详细描述

Shen-Mai-San could improve fatigue, general weakness, neutropenia for patients under going chemotherapy or radiotherapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Postoperative patients with histologically confirmed cancer within 3 years and undergoing chemotherapy or radiotherapy
  • age above 18 years old
  • signed informed consent
  • ability to read Chinese, ability for oral intake.

排除标准

  • being pregnancy
  • on breast feeding
  • completed chemotherapy or radiotherapy
  • brain metastasis with Eastern Cooperative Oncology Group (ECOG) performance status of two to four
  • delusion or hallucination
  • acute infection
  • received medications for other clinical trials.

研究组 & 干预措施

Shen-Mai San

Active Comparator

Shen mai san is composed of three herb medicines, Ginseng radis, Liriope spicata, and Schizandrae fructus and was manufactured into concentrated herbal extract and packed with 0.5g per capsule and labeled by Sun-Ten pharmaceutical company in Taiwan with good manufacturing practice (GMP).

干预措施: Shen-Mai San (Drug)

starch

Placebo Comparator

Starch in the same granule as intervention group for this double-blind trial

干预措施: Starch (Drug)

结局指标

主要结局

Change from baseline in EORTC QOL-C30 at four weeks

时间窗: baseline and four weeks

次要结局

  • Change from baseline in BUN, Creatinine, GOT, GPT at four weeks(baseline and four weeks)
  • Change from baseline in Heart rate variability at four weeks(baseline and four weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chia-Yun Chen

MD

Changhua Christian Hospital

研究点 (1)

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