Actively Recruiting

Age: 18Years +
All Genders
ID06472310

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

On this page

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

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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