Severe exacerbations predict excess lung function decline in asthma.
T R Bai, J M Vonk, D S Postma...
https://pubmed.ncbi.nlm.nih.gov/17537763/Actively Recruiting
Led by Beijing Chao Yang Hospital · Updated on 2023-07-10
400
Participants Needed
1
Research Sites
52 weeks
Total Duration
Researchers are conducting a prospective observational study to establish a standardized asthma cohort in China, involving 400 patients diagnosed with asthma according to the 2023 GINA criteria. The study aims to build an information network platform and a biospecimen bank to observe asthma outcomes and identify biomarkers that may predict these outcomes. The research is designed to explore the mechanisms behind asthma and find treatable traits related to disease progression. Participants will undergo diagnostic tests such as lung function tests, chest CT scans, induced sputum analysis, blood routine tests, IgE tests, FeNO tests, six-minute walk tests, and complete asthma-related questionnaires. These procedures follow routine diagnosis and treatment protocols. Blood samples will be collected and sent to designated laboratories for storage and biomarker analysis. No additional investigational drugs will be administered during the study. Patients will be followed for two or more years, with baseline and follow-up data collected regularly. Outcome measures include the Asthma Control Test ACT, Asthma Control Questionnaire ACQ, and induced sputum analysis over two years. Researchers will monitor prognosis prediction related to specific treatment regimens. Data will be entered electronically and on paper questionnaires, with oversight by the principal investigator and analysis by a dedicated epidemiology and statistics team. The total participation duration is at least two years.
CONDITIONS
The Cohort Study for Asthma in China
M
Meishan Liu, M.D.
Y
Ying Wang, M.D.
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Beijing Chao Yang Hospital
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Baseline
Participants undergo diagnostic tests including lung function test, chest CT, induced sputum, blood routine test, IgE test, FeNO test, six minutes walk test, and complete questionnaires for asthma as part of routine diagnosis and treatment.
1 visit (in-person)
Duration - 2 or more years
Participants are followed up for 2 or more years to monitor asthma control and disease outcomes through assessments such as Asthma Control Test, Asthma Control Questionnaire, and induced sputum analysis.
Periodic visits over 2 years
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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Lead Sponsor