跳至主要内容
临床试验/NCT04183530
NCT04183530招募中不适用

The Individualized Accurate Diagnosis and Treatment, as Well as the Prevention of Acute Exacerbation of Chronic Objective Pulmonary Disease(COPD) Based on Multidimensional Data

Wuhan Union Hospital, China1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2019年10月16日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,000
试验地点
1
主要终点
The metabolomics analysis of participates' urine or stool

研究概览

简要总结

Chronic obstructive pulmonary disease (COPD) is known as progressive lung disease and the fourth leading cause of death worldwide. Despite valuable efforts, there is still no Individualized accurate diagnostic and prognostic tool for COPD. Hence, the investigators' research integrated multi-dimensional data of COPD patients, which may provide an invaluable bioinformatic resource for understanding the underlying molecular alterations that drive disease progression, with the goal of developing individualized accurate diagnostic and therapeutic inventions.

详细描述

Chronic obstructive pulmonary disease (COPD) is known as progressive lung disease and the fourth leading cause of death worldwide. Acute exacerbations of COPD (AECOPD) is an important event of disease progression worsening in airway function and respiratory symptoms, bringing about respiratory failure, and increasing the rates of mortality. Despite valuable efforts, there is still no Individualized accurate diagnostic and prognostic tool for COPD. In this context, the investigators are to perform comprehensive transcriptomic, proteomic, metabonomic and exosome characterization of COPD patients and healthy controls. Biological samples of COPD participants, including blood, urine, stool, saliva, bronchoalveolar lavage fluid and clinical characteristics are going to be collected from the remaining materials of the routine clinical examination. And samples of healthy controls will be collected from the rest of the healthy examination practice. By integrating the multi-dimensional data, the investigators aim to elucidate the impact of molecular alterations driving phenotypic variation and to delineate the mechanisms of AECOPD for prospective exploration of personalized, precision-based clinical care.

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
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient has signed informed consent.
  • Patients diagnosed with COPD or fully healthy participants.

排除标准

  • Tumor disease.
  • Heart disease.
  • Thyroid disease.

结局指标

主要结局

The metabolomics analysis of participates' urine or stool

时间窗: through study completion, an average of 1 year

Predominately include metabolic target analysis, metabolic profiling analysis

The transcriptome analysis of participates' serum or plasma

时间窗: through study completion, an average of 1 year

Include the transcriptome data of serum,plasma or exosomes inside

The proteomics analysis of bronchoalveolar lavage fluid and saliva

时间窗: through study completion, an average of 1 year

Differentially expressed proteins between SCOPD and AECOPD which associated with disease progression were analyesd

次要结局

未报告次要终点

研究者

发起方
Wuhan Union Hospital, China
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yang Jin

Professor

Wuhan Union Hospital, China

研究点 (1)

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