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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05376618
Other study ID # 2021-KY-060--01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 15, 2021
Est. completion date July 15, 2022

Study information

Verified date July 2021
Source Zhujiang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Chronic obstructive pulmonary disease (COPD), a common and complex disease characterized by persistent airflow limitation, is a leading cause of mortality worldwide. COPD and its comorbidity are associated with hypoxia condition. Further investigations on the cellular and molecular aspects of hypoxia in COPD should help to reveal the mechanisms underlying the development of this disease. Dysfunction of the erythrocyte, a main medium to transport oxygen through the blood, contributes to the prognosis and severity of COPD through hypoxia. It is proposed that dysregulated proteins in erythrocytes that impair oxygen transport may be involved in the development of COPD. However, a comprehensive study on altered proteins of erythrocytes in COPD is still lacking. Proteomics techniques and protein chip techniques provide a high throughput screening method to figure out characteristic inflammatory or metabolic markers of diseases. Therefore, this study is to evaluate the clinical significance of differential erythrocyte proteins in the course of COPD disease.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date July 15, 2022
Est. primary completion date July 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 80 Years
Eligibility 1. case group Inclusion Criteria: 1. Age from 40 to 80 years old; gender is not limited. 2. Stable COPD 3. Sign the informed consent with the willingness of obeying the protocol. - Exclusion Criteria: 1. Subjects with known other chronic respiratory diseases except for COPD (such as asthma, tuberculosis, bronchiectasis, interstitial lung disease, occupational lung diseases, sarcoidosis, lung cancer, et al); 2. Subjects had been accepted lung lobectomy or transplantation; 3. Subjects be ill with severe, or uncontrolled systemic diseases other than COPD (such as psychiatry diseases, chronic liver diseases, heart failure, auto-immunity diseases, chronic renal diseases, et al ); 4. Alcoholism, drug or solvents addition; 5. Acute exacerbation COPD patients (AECOPD) - 2. control group Inclusion criteria 1. Age from 40 to 80 years old; gender is not limited. 2. Sign the informed consent with the willingness of obeying the protocol. - Exclusion criteria 1. Subjects with known other chronic respiratory diseases (such as COPD, asthma, tuberculosis, bronchiectasis, interstitial lung disease, occupational lung diseases, sarcoidosis, lung cancer, et al); 2. Subjects had been accepted lung lobectomy or transplantation; 3. Subjects be ill with severe, or uncontrolled systemic diseases other than COPD (such as psychiatry diseases, chronic liver diseases, heart failure, auto-immunity diseases, chronic renal diseases, et al ); 4. Alcoholism, drug or solvents addition;

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
no intervention

Locations

Country Name City State
China Zhujiang Hospital,Southern Medical Universtiy Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Zhujiang Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Protein biomarkers in erythrocyte predicting rapid decline of lung function The study is to identify the biomarkers and make sure which is associated with rapid decline of lung function. The study will include a total of 30 study subjects. 2021-7-15 to 2022-7-15
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