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临床试验/NCT04863274
NCT04863274已完成不适用

The Program to Assess the Influence of Routing and In-depth Consultation of Patients With Cardiovascular Risk Factors on the Choice of Medicine and Treatment Compliance

The League of Clinical Research, Russia1 个研究点 分布在 1 个国家目标入组 2,912 人开始时间: 2018年6月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
2,912
试验地点
1
主要终点
Target level of LDL cholesterol

研究概览

简要总结

A systematic collection of retrospective and prospective data based on non-interventional patient observation, aimed to assess the risks, course and outcomes of a disease or a group of diseases:

  • the retrospective part: database of patients with cardiovascular risks;
  • the prospective part: observation of patients in the real world medical practice.

详细描述

The research program will have two parts:

Stage 1: identification of patients with moderate, high and very high cardiovascular risk, not having diseases of atherosclerotic genesis and requiring lipid-lowering drugs.

Stage 2: a prospective observation of patients receiving primary medical prophylaxis of CVD with atorvastatin.

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
40 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Expanded consultation group

In an expanded consultation group is being conducted in the study group on the importance of primary prevention of cardiovascular diseases and on the reduction of cardiovascular risk by taking statins. Patients are given brochures and information materials on the risk factors for cardiovascular diseases and the possibility of their correction. Also, the patients of the study group are regularly reminded (2 times a month) with the help of SMS mailings and calls of health workers about the need to follow the doctor's recommendations for taking atorvastatin and returning to the medical institution.

干预措施: atorvastatin (Drug)

结局指标

主要结局

Target level of LDL cholesterol

时间窗: 12 months

To assess number of patients achieving the target level of low-density lipoprotein cholesterol in study group and in control group.

次要结局

未报告次要终点

研究者

发起方
The League of Clinical Research, Russia
申办方类型
Other
责任方
Sponsor

研究点 (1)

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