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NCT03240315Active, not recruiting

Personalized Prediction Strategy for Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Establishment of Individualized Prediction System for Acute Exacerbation of Chronic Obstructive Pulmonary Disease Based on Cloud Platform

Source: ClinicalTrials.gov · Last updated 12 Jan 2026

Brief summary (registry, in English)

This is a 3-year longitudinal study designed to establish a personalized prediction and prevention system for acute exacerbations of chronic obstructive pulmonary disease (AECOPD). Data will be prospectively collected from patients with chronic obstructive pulmonary disease (COPD) and healthy control participants, including clinical characteristics, pathophysiological parameters, etiological factors, and immunological information. These data will be analyzed using data mining approaches combined with Internet-based technologies.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
442 (actual)
First submitted
31 Jul 2017
Start date
1 Aug 2016
Primary completion date
30 Sept 2026
Lead sponsor
Guangzhou Institute of Respiratory Disease
Diseases
COPD
NCT number
NCT03240315

What you commit to

  • Study type: Observational
  • Participants enrolled: 442
  • From 1 Aug 2016 to the primary completion date, 30 Sept 2026
  • 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

  • A COPD subject will not be eligible for inclusion in this study if any of the following criteria apply:
    • Known respiratory disorders, or disorders identified at screening/visit 1 (including identification on the first CT scan), other than COPD (e.g.: lung cancer, sarcoidosis, tuberculosis, lung fibrosis, cystic fibrosis)
    • Known history of significant inflammatory disease, other than COPD (e.g. rheumatoid arthritis and Lupus)
    • Known to be severely alpha-1-antitrypsin deficient
    • Has experienced a moderate or severe exacerbation (requiring oral corticosteroid, antibiotics or hospitalisation) within the last 4 weeks
    • Having undergone lung surgery (e.g. lung reduction, lung transplant)
    • Have cancer or have had cancer in the 5 years prior to study entry
    • Having received a blood transfusion in the 4 weeks prior to study start
    • Inability to walk
    • Taking part in a blinded drug study
    • Having therapy with systemic corticosteroids at inclusion.

Who the study is looking for

  • Patients was diagnosed as COPD according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines older than 40 years old.
    • A signed and dated written informed consent is obtained prior to participation.
    • Able to comply with the requirements of the protocol and be available for study visits over 3 years.

Age in the registry: 40 years to - · 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
Guangzhou Institute of Respiratory Health,The First Affiliated Hospital of Guangzhou Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status

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