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
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