Actively Recruiting
Chronic Airway Disease and Multimorbidity Cohort
Led by China-Japan Friendship Hospital · Updated on 2025-02-17
2000
Participants Needed
9
Research Sites
182 weeks
Total Duration
On this page
Sponsors
C
China-Japan Friendship Hospital
Lead Sponsor
S
Second Affiliated Hospital of Xi'an Jiaotong University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Background: Chronic airway diseases (CAD), including chronic obstructive pulmonary disease (COPD), asthma and bronchiectasis, are highly prevalent and cause serious disease burden. Multimorbidity is recognized to influence treatment decision and prognosis of patients with stable CAD. The impact of multimorbidity on exacerbation CAD is under investigated. Methods: The Chronic Airway Disease and Multimorbidity (CAM) cohort study is a prospective, multicenter, observational study aiming to recruit a minimum of 2000 patients hospitalized for exacerbation of COPD, asthma or bronchiectasis. Comprehensive data, including demographics, medical history, comorbidities, lung function, echocardiography, microbiological profiles, radiology, quality of life and treatment will be collected at baseline during the hospitalization. Follow-up data indicating the impact of both CAD and multimorbidity will be collected at 1-, 3-, 6-, 9- and 12-months after hospital discharge. Biospecimens, including blood and bronchoalveolar lavage fluid, will be collected and analyzed for biomarker detecting. Primary outcome are length of hospital stay and re-exacerbation during fellow-up. Secondary outcomes include comorbidity pattern and its impact on respiratory symptoms burden, quality of life, pulmonary function and chest imaging as well as cost and healthcare utilization. Conclusions: The knowledge generated from CAM cohort study will fill crucial gaps in understanding how multimorbidity affects CAD and facilitate evidence-based clinical practice in the future.
CONDITIONS
Official Title
Chronic Airway Disease and Multimorbidity Cohort
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with chronic obstructive pulmonary disease aged 40 years or older; patients with asthma and bronchiectasis aged 18 years or older
- Hospital admission for acute exacerbation of COPD, uncontrolled asthma, or acute exacerbation of bronchiectasis as the primary diagnosis
You will not qualify if you...
- Unable to perform spirometry during stable periods
- Expected survival less than one month
- Refusal to sign informed consent
- Chest imaging showing new patchy infiltrates, solid shadows, ground glass shadows, interstitial changes, with or without pleural effusion
- Diagnosis of cystic fibrosis, interstitial lung disease, or other lung diseases with tractional bronchial dilatation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 9 locations
1
National Center for Respiratory Medicine, China-Japan Friendship Hospital
Beijing, Beijing Municipality, China, 100029
Actively Recruiting
2
Zhujiang Hospital of Southern Medical University
Guangzhou, Guangdong, China, 510280
Actively Recruiting
3
Henan Provincial People's Hospital
Zhengzhou, Henan, China, 450003
Actively Recruiting
4
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, China, 430022
Actively Recruiting
5
The Second Xiangya Hospital of Central South University
Changsha, Hunan, China, 410011
Actively Recruiting
6
The First Affiliated Hospital of China Medical University
Shenyang, Liaoning, China, 110001
Actively Recruiting
7
The Second Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi, China, 710114
Actively Recruiting
8
Ruijin Hospital Affiliated to Shanghai Jiao Tong University
Shanghai, Shanghai Municipality, China, 200025
Actively Recruiting
9
West China Hospital of Sichuan University
Chengdu, Sichuan, China, 610041
Actively Recruiting
Research Team
K
Ke Huang, MD.
CONTACT
W
Wei Li, MD.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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