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临床试验/NCT05000541
NCT05000541已完成不适用

Observation of the Effects of Guideline-driven Lifestyle Interventions, Including Use of a Red-yeast Based Nutraceutical , in Subjects With Hypercholesterolemia at Low-moderate Cardiovascular Risk Not Requiring a Drug Therapy

Mylan Inc.3 个研究点 分布在 2 个国家目标入组 259 人开始时间: 2020年12月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Mylan Inc.
入组人数
259
试验地点
3
主要终点
Mean change from baseline in LDL-C

研究概览

简要总结

The objective of the present multinational, multicentre, prospective, scientific study is to confirm that prescription of a low-dose red yeast-based nutraceutical.

详细描述

The objective of the present multinational, multicentre, prospective, scientific study is to confirm that prescription of a low-dose red yeast-based nutraceutical significantly increases the LDL-C lowering effect of guideline-driven lifestyle interventions in subjects with hypercholesterolemia at low-moderate cardiovascular risk not requiring a drug therapy.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
25 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 25 and 75 years;
  • In primary prevention for low-moderate CV risk, with diet and physical exercise to control raised LDL-C level, for at least 3 months;
  • LDL-C > 100 mg/dL (2.6 mmol/L), < 190 mg/dL (4.9 mmol/L)
  • CV risk SCORE <5% (based on SCORE chart according to figure I for Poland respective figure 2 for Austria and Germany in the ESC/EAS guideline 2019);
  • Triglyceride <400 mg/dL;
  • Advised to use nutraceutical as part of the lifestyle intervention as per guideline and within the product label (i.e. posology as in product label);
  • Written informed consent.

排除标准

  • Subjects being treated or who have been treated for up to 3 months before the start of the study with lipid-lowering drugs or nutraceuticals including functional foods for which lipid-lowering effects are known (e.g. fish oil, sterol-containing yoghurts etc.);
  • Subjects involved in other clinical studies with pharmaceutical products
  • Known laboratory evidence of either liver, muscle, thyroid or kidney dysfunction;
  • Subjects with prior history of cardiovascular events or with high cardiovascular risk equivalents;
  • Uncontrolled hypertension (systolic blood pressure >190 mmHg or diastolic blood pressure >100 mmHg);
  • Pregnancy and breastfeeding.

结局指标

主要结局

Mean change from baseline in LDL-C

时间窗: 3 months

Mean change from baseline in LDL-C at 3 months

次要结局

  • Subjects' adherence to the prescribed lifestyle interventions measured on Visual Analogue Scale (VAS)(at 3 months and 6 months)

研究者

发起方
Mylan Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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