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An Observational Multicenter Cross-sectional Study of Patients With Uncontrolled Severe Asthma in Russia
Led by AstraZeneca · Updated on 2026-05-07
5000
Participants Needed
37
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Researchers are conducting an observational multicenter cross-sectional study involving 5,000 adult patients with uncontrolled severe asthma (SA) across approximately 50 outpatient centers in Russia. The study aims to describe the characteristics of patients with uncontrolled SA not receiving biologic treatments, addressing the lack of unified monitoring and epidemiological data for this population in Russia. This research is important to better understand the clinical and demographic features, treatment patterns, and outcomes of SA across different regions with diverse populations and environments. This non-interventional study involves only one visit per participant to collect demographic and clinical data without altering routine medical care or adding diagnostic or therapeutic procedures beyond standard practice. Patients receiving biologic therapies are excluded, focusing on those treated with standard care such as inhaled corticosteroids, long-acting bronchodilators, and systemic corticosteroids. The study will evaluate the use of routine therapies, patterns of oral corticosteroid prescriptions, and associated clinical characteristics including comorbidities and biomarkers. Participants will provide data from their medical records covering at least 52 weeks prior to inclusion, allowing researchers to analyze treatment changes, exacerbation rates, lung function, and healthcare resource use retrospectively. The study will collect information on demographics, asthma control scores, eosinophil counts, immunoglobulin E levels, and other clinical measures. Data collection spans from June 2024 to June 2027, with no interventions or additional monitoring beyond routine care, offering a comprehensive profile of uncontrolled SA in Russia.
CONDITIONS
Brief Title
Clinical and demOgRaphic Features of Patients With Uncontrolled Severe Asthma in Russia (CORSAR)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older at the time of inclusion
- Signed informed consent before joining the study
- Diagnosis of uncontrolled severe asthma with ACQ-5 score greater than 1.5 for at least 52 weeks prior
- Severe asthma treated with medium or high doses of inhaled corticosteroids plus other therapies for at least 3 months before inclusion
- At least 52 weeks of follow-up data available in medical records prior to inclusion
You will not qualify if you...
- Current or past 52 weeks use of biological therapy
- Diagnosis or history of chronic obstructive pulmonary disease (COPD) or idiopathic pulmonary fibrosis (ILF)
- Participation in any clinical study currently or within the past 52 weeks
- Presence of acute or chronic disease limiting study participation or affecting result interpretation as judged by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants with uncontrolled severe asthma not receiving biological therapy are observed to collect clinical and demographic data in a single visit.
1 visit (in-person)
Trial Site Locations
Total: 37 locations
1
Research Site
Astrakhan, Russia
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2
Research Site
Barnaul, Russia
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3
Research Site
Blagoveshchensk, Russia
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4
Research Site
Bryansk, Russia
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5
Research Site
Chelyabinsk, Russia
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6
Research Site
Gatchina, Russia
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7
Research Site
Irkutsk, Russia
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8
Research Site
Izhevsk, Russia
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9
Research Site
Kazan', Russia
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10
Research Site
Kemerovo, Russia
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11
Research Site
Khabarovsk, Russia
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12
Research Site
Krasnodar, Russia
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13
Research Site
Krasnoyarsk, Russia
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14
Research Site
Moscow, Russia
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15
Research Site
Murmansk, Russia
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16
Research Site
Nal'chik, Russia
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17
Research Site
Nizhny Novgorod, Russia
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18
Research Site
Novosibirsk, Russia
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19
Research Site
Omsk, Russia
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20
Research Site
Orenburg, Russia
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21
Research Site
Petrozavodsk, Russia
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22
Research Site
Rostov-on-Don, Russia
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23
Research Site
Ryazan, Russia
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24
Research Site
Saint Petersburg, Russia
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25
Research Site
Samara, Russia
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26
Research Site
Saratov, Russia
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27
Research Site
Stavropol, Russia
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28
Research Site
Tomsk, Russia
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29
Research Site
Ufa, Russia
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30
Research Site
Ulan-Ude, Russia
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31
Research Site
Verkhnyaya Pyshma, Russia
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32
Research Site
Vladimir, Russia
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33
Research Site
Vladivostok, Russia
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34
Research Site
Volgograd, Russia
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35
Research Site
Voronezh, Russia
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36
Research Site
Yakutsk, Russia
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37
Research Site
Yekaterinburg, Russia
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Research Team
A
AstraZeneca Clinical Study Information Center
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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