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临床试验/KCT0005460
KCT0005460尚未招募未知

A Clinical Trial to Analyze the effect of oral intake of Phellinus linteus(sanghuang) Extract on immune function: Randomized, Double-blind Controlled Trial

Cheonan Korean Medicine Hospital of Daejeon University0 个研究点目标入组 98 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
98

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
20(Year) 至 65(Year)(—)
性别
All

入选标准

  • 1. Men and women aged 20 to 65 years old
  • 2. Peripheral blood WBC of 3×1000/µl or more and less than 10×1000/µl
  • 3. Those who have had upper respiratory tract infections or cold symptoms, a typical disease that can cause upper respiratory tract infections, more than two times within one year before the start of the test
  • 4. A person who has agreed to participate in this test and signed a written consent form by the subject (or legal representative) voluntarily

排除标准

  • 1. Those who are currently being treated for clinically significant acute or chronic cardio-cerebrovascular system, immune system, respiratory system, hepatobiliary system, kidney and urinary system, nervous system, musculoskeletal disease, psychotic, infectious and hematologic/neoplastic diseases, etc. You can participate in the research at the discretion of the research director considering the status of
  • 2. Those with uncontrolled hypertension (160/100mmHg or more, measured after 10 minutes of rest for the subject)
  • 3. Patients with uncontrolled diabetes (fasting glucose 126mg/dL or higher, or starting a new drug due to diabetes within 3 months)
  • 4. Those whose AST(GOT) or ALT(GPT) blood level is 3 times or more than the normal upper limit of the relevant organ7,8,9
  • 5. Creatinine blood levels exceeding 2.4mg/dL for men and 1.8mg/dL for women
  • 6. Those who have consumed or are ingesting health functional foods that may affect immunity within 2 weeks before screening
  • 7. Those who complain of severe gastrointestinal symptoms such as heartburn and indigestion
  • 8. Pregnant, lactating or planning to become pregnant during the study period
  • 9. Those who are sensitive or allergic to test food related foods
  • 10. Those who plan to participate in other studies during this study
  • 11. Those who received other study drugs within 4 weeks of starting this study
  • 12. Those who the researcher deems unsuitable for this study

研究者

发起方
Cheonan Korean Medicine Hospital of Daejeon University

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