Predictive Value of Inflammatory Biomarkers and FEV1 for COPD

NCT03532893 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10385

Last updated 2022-03-29

No results posted yet for this study

Summary

This is a multi-center, prospective, cohort study. A total of 10,000 people aged 40~75 without lung disease will be recruited and followed for 3 years. By measure the rate of decline in forced expiratory volume at one second(FEV1) and baseline inflammatory biomarkers in exhaled breath condensate and peripheral blood, we aim to explore the predictive model for chronic obstructive pulmonary disease(COPD) in China.

Conditions

Interventions

OTHER

No intervention

This is a multi-center,observational, prospective, cohort study. A total of 10,000 subjects aged 40~75 without history of lung disease will be recruited and followed for 3 years. So there is no intervention in this study.

Sponsors & Collaborators

  • The Second Hospital of Hebei Medical University

    collaborator OTHER
  • Henan Provincial People's Hospital

    collaborator OTHER
  • Second Hospital of Jilin University

    collaborator OTHER
  • First Affiliated Hospital Xi'an Jiaotong University

    collaborator OTHER
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • Shanxi Dayi Hospital

    collaborator OTHER
  • Tianjin Medical University General Hospital

    collaborator OTHER
  • The Affiliated Hospital of Inner Mongolia Medical University

    collaborator OTHER
  • The First Hospital of Qinhuangdao

    collaborator OTHER_GOV
  • Peking University First Hospital

    lead OTHER

Principal Investigators

  • Guangfa Wang, MD · Peking University First Hospital

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-03-03
Primary Completion
2020-12-31
Completion
2021-10-09

Countries

  • China

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03532893 on ClinicalTrials.gov