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NCT03044847Enrolling by invitation

The Cohort Study for Chronic Obstructive Pulmonary Disease (COPD) in China

The Cohort Study for Chronic Obstructive Pulmonary Diseases (COPD) in China---- Observation of the Disease Outcome and Identification of Prognostic Biomarkers for the Disease Outcome

Source: ClinicalTrials.gov · Last updated 29 Jul 2021 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study is to establish the large COPD cohort and biological database in China, aiming for precision medicine to optimize diagnosis and treatment choices and to monitor and improve clinical outcomes in this disease.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
3800 (estimated)
First submitted
25 Jan 2017
Start date
1 Jul 2016
Primary completion date
31 Dec 2028
Lead sponsor
Beijing Chao Yang Hospital
Diseases
COPD
NCT number
NCT03044847

What you commit to

  • Study type: Observational
  • Planned participants: 3800
  • From 1 Jul 2016 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • thoracic or abdominal surgery in the last 3 months
  • eye surgery in the last three months

Other illness

  • Having other respiratory diseases with massive lung tissue destruction such as severe bronchiectasis and tuberculosis, etc
  • The usual criteria of serious uncontrolled diseases
  • myocardial infarction in the last 3 months
  • admission to hospital for any cardiac condition in the last month
  • heart rate over 120 beats per minute
  • antibacterial chemotherapy for tuberculosis

Other

  • Acute exacerbation in the past 3 months
  • retinal detachment
  • pregnant or breast feeding

Who the study is looking for

  • Aged 40-75 years
  • COPD group: baseline post-bronchodilator FEV1/FVC \< 0.7
  • GOLD 0 group: individuals with chronic respiratory symptoms and/or high risk factors
  • Signed informed consent obtained prior to participations with the ability to comply with protocol and be available for study visits over 5 years

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Capital Medical University
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.