Study identifier:D589BR00078
ClinicalTrials.gov identifier:NCT06172777
EudraCT identifier:N/A
CTIS identifier:N/A
A study to evaluate the consistency of oscillometry and spirometry test results in patients with confirmed or suspected asthma or COPD
asthma/ COPD
N/A
No
-
All
72
Observational
18 Years - n/a
Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Sept 2024 by AstraZeneca
AstraZeneca
-
The study to evaluate the consistency of oscillometry and spirometry test results in patients with confirmed or suspected asthma or COPD, it is a multi-centre clinical study. sponsor by Astrazeneca Investment(China) Co.,LTD.
800 patients, including suspected or confirmed asthma, suspected or confirmed COPD, will be enrolled in nationwide multiple study centres. Enrolling suspected and confirmed subject in an approximate1:1 rate in centre-level. About 100 subjects were enrolled at the leader site, while about 14 subjects were enrolled at other sites. To evaluate the consistency of oscillometry and spirometry test results in patients with confirmed or suspected asthma or COPD.
Arms | Assigned Interventions |
---|---|
suspected asthma enrollment 200 subjects | Diagnostic Test: suspected asthma enrollment 200 asthma patients |
Suspected COPD enrollment 200 subjects | Diagnostic Test: suspected COPD enrollment 200 COPD patients |
confirmed asthma enrollment 200 subjects | Diagnostic Test: confirmed asthma enrollment 200 patients |
confirmed COPD enrollment 200 subjects. | Diagnostic Test: confirmed COPD enrollment 200 patients |
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