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临床试验/NCT04474717
NCT04474717已完成不适用

Clinical and Biochemical Assessment of the Course of Chronic Obstructive Pulmonary Disease in Combination With Atherosclerosis

Ryazan State Medical University2 个研究点 分布在 1 个国家目标入组 476 人开始时间: 2020年11月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
476
试验地点
2
主要终点
mortality

研究概览

简要总结

one-centered, open, non-randomized, controlled clinical trial will focus on a comprehensive study of the clinical, functional and molecular biochemical characteristics of the natural course of COPD in combination with peripheral atherosclerosis

详细描述

Risk factors, chronic respiratory symptoms and respiratory function in the natural history of COPD will be monitored. In a group of patients with a comorbid course of COPD and atherosclerosis, systemic inflammation and its molecular mechanisms will be investigated. Also in this group, the role of non-coding miRNAs will be analyzed. The study also includes an analysis of the clinical and biochemical COPD phenotype with systemic inflammation and comorbidity.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

入排标准

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

入选标准

  • A significant diagnosis of COPD, confirmed by spirometry criteria, typical clinical presentation.
  • A significant diagnosis of peripheral atherosclerosis
  • The high level of adherence to treatment
  • Signed informed agreement

排除标准

  • The presence of other chronic respiratory diseases in the patient, including bronchial asthma
  • Known oncological diseases of any localization
  • HIV infection and other immunodeficiency conditions
  • Inability to understand and comply with the requirements of the research protocol.

结局指标

主要结局

mortality

时间窗: 12 months

the number of deaths from cardiovascular causes

exacerbations

时间窗: 12 months

frequency of exacerbations of COPD (number of cases per year)

markers of inflammation

时间窗: 12 months

biochemical markers of inflammation (IL-6, pg/ml; IL-8,pg/ml;TNF,pg/ml)

lung function

时间窗: 12 months

progression of decreased lung function (FEV1%) according to spirometry

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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