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临床试验/KCT0008540
KCT0008540招募中Unknown

A 8 weeks, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Saccaharum Officinalis L. wax alcohols(Policosanol) on improvement of blood cholesterol

Wonkwang University, Gwangju Medical Center0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
100

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
19(Year) 至 75(Year)(—)
性别
All

入选标准

  • 1) Men and women aged 19 ~ 75
  • 2) LDL-cholesterol 140~189 mg/dL and total cholesterol ≥ 200 mg/d

排除标准

  • 1. a person who has taken lipid lowering agent study within 6 months before the screening test.
  • 2. BMI < 18.5 kg/m^2 or, ≥ 35 kg/m^2
  • 3. fasting glucose level ≥ 140 mg/dL
  • 4. a person who is taking on diabetes medication or out of control hypertension(Systolic Blood Pressure ≥140 mmHg OR Diastolic Blood Pressure ≥100 mmHg)
  • 5. Subjects who are sensitive to Saccaharum Officinalis L. wax alcohols(Policosanol)
  • 6. have a Coagulation disorder or, taking anticoagulant, antithrombotic.
  • 7. a person who has experience in antipsychotic medication within 3 months before the screening test.
  • 8. history of alcoholism or substance abuse
  • 9. Pregnant or lactating women
  • 10. fertile women without proper contraceptives
  • 11. Participation in other human study within 3 months before the screening test.

研究者

发起方
Wonkwang University, Gwangju Medical Center

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