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Recruiting Not applicable NCT06909773

The Prevalence, Disease Burden and Prognosis of COPD in Patients With Cardiovascular Diseases

No applicable phase (e.g. observational)
Conditions: Cardiovascular Diseases

Sponsor: AstraZeneca

trial.available_in: БГ
Overview
This is a multi-center, prospective, and interventional study conducted in 3 types of cardiovascular diseases (CVD) subjects , including 3 cohorts which are patients with newly or previously diagnosed coronary heart disease ( CHD), atrial fibrillation ( AF) and chronic heart failure (CHF).
Description
The mainly purpose of this study is describe the prevalence of COPD of the subjects with 3 types of CVD who are aged 40 years or older, and also observe the effect of cardiopulmonary co management on the short term prognosis of subjects with CVD and COPD. This study will enroll approximately 3,000 subjects, with approximately 1,000 subjects in each cohort.
Who can participate
Inclusion Criteria: 1. Give signed written informed consent to participate. 2. At least 40 years of age at baseline visit. 3. Previous or newly diagnosed by at least one of the 3 types of CVD which are, * Coronary heart disease ( CHD ) * Atrial fibrillation (AF ) * Chronic heart failure ( CHF ) 4. Subjects have no absolute contraindications to spirometry testing. 5. Subjects have the cognitive ability to conduct questionnaires after e valuated by investigators. Exclusion Criteria: 1. Significant diseases or conditions, which, in the opinion of the investigator, may put the subject at risk because of participation in the study or may influence either the results of the study or the subject's ability to participate in the study. 2. Women who are pregnant or lactating or are planning to become pregnant, or women of childbearing potential who are not using an acceptable method of contraception. 3. Subjects who are not able to provide written informed consent. 4. Treatment with investigational study drug or device in another clinical study within the last 30 days or five half lives prior to baseline visit , whichever is longer.
Interventions
Guideline education and implementation intervention
BEHAVIORAL
Locations 84
China (84)
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Anqing
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Beijing
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Beijing
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Beijing
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Beijing
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Beijing
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Changsha
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Changsha
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Chaohu
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Chengdu
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Chengdu
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Chengdu
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Chifeng
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Chongqing
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Dalian
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Dingzhou
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Dongguan
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Foshan
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Fuyang
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Fuzhou
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Ganzhou
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Guanghan
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Guangzhou
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Guangzhou
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Guangzhou
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Guangzhou
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Haikou
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Hangzhou
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Hangzhou
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Harbin
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Harbin
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Hefei
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Hefei
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Hubei
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Jinhua
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Jinzhong
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Jiujiang
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Kaiyuan
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Kunming
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Kunming
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Lanzhou
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Leping
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Lianjiang
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Linhai
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Meizhou
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Mianyang
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Nanchang
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Neijiang
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Ningbo
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Ningbo
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Putian
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Quanzhou
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Shanghai
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Shanghai
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Shanghai
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Shanghai
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Shanghai
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Shantou
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Shantou
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Shenyang
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Shenzhen
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Shijiazhuang
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Suining
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Suzhou
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Tai’an
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Taiyuan
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Taiyuan
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Tianjin
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Tianjin
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Tianjin
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Tianmen
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Wuhan
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Wuhan
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Wuxi
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Xi'an
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Xiamen
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Xiangyang
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Xinzheng
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Xuzhou
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Yangzhou
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Yulin
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Zhangzhou
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Zhengzhou
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Zunyi
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
40 Years
Healthy volunteers
No
Start date
28.11.2025
Completion date
31.12.2026
Registry ID
NCT06909773
Source
clinicaltrials.gov
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