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临床试验/NCT01742000
NCT01742000已完成3 期

Double-blinded Placebo-controlled Study of Anti-atherosclerotic Activity of Karinat in Postmenopausal Women

Institute for Atherosclerosis Research, Russia0 个研究点目标入组 180 人开始时间: 2007年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
180
主要终点
B-mode ultrasound of carotid arteries

研究概览

简要总结

The purpose of this study is to investigate the anti-atherosclerotic action of natural drug Karinat based on phytoestrogen-rich botanicals in postmenopausal women.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Care Provider)

入排标准

性别
Female
接受健康志愿者

入选标准

  • Women at least 5 years after menopause
  • Maximum intima-media thickness of common carotid artery more than 0,80 mm (ultrasonographic B-mode examination)
  • The absence of climacteric syndrome (less than 3 points by Blatt-Kupperman scale)
  • The absence of chronic diseases demanding permanent drug administration (more than 2 month per year)
  • The absence of hypolipidemic therapy or hormone replacement therapy during 6 months before the inclusion

排除标准

  • Administration of lipid-lowering drugs, and/or hormone replacement therapy, and/or phytoestrogens during 6 month before inclusion
  • Continuous administration of sulfonylurea derivatives, and/or beta-blockers, and/or calcium antagonists (more than 2 months per year)
  • Personal history or diagnostic of following diseases:
  • Personal history of stroke, coronary heart disease, acute myocardial infarction or transient ischemic attacks
  • Pulmonary thromboembolism
  • Chronic heart failure IIa-III
  • Uncontrolled arterial hypertension (systolic blood pressure > 145 mmHg, diastolic blood pressure > 95 mmHg under hypotensive therapy)
  • Chronic renal failure II-III
  • Chronic hepatic failure II-III
  • Liver cirrhosis
  • Individual intolerance of Karinat or major side effects

研究组 & 干预措施

Karinat

Active Comparator

Karinat 500 mg tablet by mouth three times a day

干预措施: Karinat (Dietary Supplement)

Sugar pill

Placebo Comparator

Placebo 500 mg tablet by mouth three times a day

干预措施: Placebo (Drug)

结局指标

主要结局

B-mode ultrasound of carotid arteries

时间窗: up to 2 years

Variation of intima-media thickness of common carotid arteries

次要结局

  • Measure of serum atherogenicity(up to 2 years)

研究者

发起方
Institute for Atherosclerosis Research, Russia
申办方类型
Other
责任方
Sponsor

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