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Study of Patient With Frequent COPD Exacerbations
RECRUITINGSponsored by AstraZeneca
Actively Recruiting
SponsorAstraZeneca
Started2024-12-16
Est. completion2026-06-30
Eligibility
Age18 Years – 100 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT07221981
Summary
This Study is a multicenter, non-interventional, observational, ambispective (retrospective-prospective) study to evaluate clinical and demographic characteristics, approaches to therapy in outpatients with COPD and frequent exacerbations in the Russian Federation. Planned number of Study site is 35 outpatient centers with experience of treatment of COPD with frequency exacerbations in about 30 regions in Russia.
Eligibility
Age: 18 Years – 100 YearsHealthy volunteers accepted
Inclusion Criteria: 1. Age ≥ 18 years at the time of inclusion; 2. Signed and dated written informed consent in accordance with ICH-GCP and local law prior to inclusion in the study; 3. Patients with diagnosed moderate-to-severe COPD (see comments below); 4. ≥2 moderate or ≥1 severe COPD exacerbations in previous 52 weeks (see comments below); 5. Patients have been receiving two inhaled maintenance therapies (LABA/LAMA, ICS/LABA, ICS/LAMA) for at least 6 weeks prior to inclusion. Exclusion Criteria: 1. Current or previous treatment with triple combination (ICS/LABA/LAMA) within 52 weeks prior to inclusion; 2. COPD due to documented α-1 antitrypsin deficiency; 3. A diagnosis of bronchiectasis, sarcoidosis, interstitial lung diseases, or idiopathic pulmonary fibrosis, exacerbation of bronchial asthma or any acute or chronic disease that, as deemed by Investigator, limits the ability of patients to participate in this study or could influence the interpretation of the results; 4. The participation in any clinical study currently or within 52 weeks prior to inclusion.
Conditions2
COPDChronic Obstructive Pulmonary Disease (COPD)
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Actively Recruiting
SponsorAstraZeneca
Started2024-12-16
Est. completion2026-06-30
Eligibility
Age18 Years – 100 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT07221981