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The Individualized Accurate Diagnosis and Treatment of Chronic Objective Pulmonary Disease(COPD) Patients Based on Multidimensional Data

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04183530
Acronym
COPD
Enrollment
1000
Registered
2019-12-03
Start date
2019-10-16
Completion date
2024-12-30
Last updated
2021-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Exacerbation of Chronic Obstructive Pulmonary Disease, Copd

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patient has signed informed consent. 2. Patients diagnosed with COPD or fully healthy participants.

Exclusion criteria

1. Tumor disease. 2. Heart disease. 3. Thyroid disease.

Design outcomes

Primary

MeasureTime frameDescription
The transcriptome analysis of participates' serum or plasmathrough study completion, an average of 1 yearInclude the transcriptome data of serum,plasma or exosomes inside
The metabolomics analysis of participates' urine or stoolthrough study completion, an average of 1 yearPredominately include metabolic target analysis, metabolic profiling analysis
The proteomics analysis of bronchoalveolar lavage fluid and salivathrough study completion, an average of 1 yearDifferentially expressed proteins between SCOPD and AECOPD which associated with disease progression were analyesd

Countries

China

Contacts

Primary ContactWei Geng, Master
dr.geng116@gmail.com+8618696152606

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026