Actively Recruiting

All Genders
ID06521229

An Ambispective Observational Multicenter Registry of Patients With Uncontrolled Asthma in Russia

Led by AstraZeneca · Updated on 2026-04-20

9000

Participants Needed

47

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying uncontrolled asthma in adults across Russia to better understand its characteristics and treatment patterns. This large-scale observational registry will include 9,000 patients from 70 outpatient centers in about 50 regions, focusing on those not receiving biologic therapy. The study aims to describe demographic and clinical features, capture complications and comorbidities, and evaluate routine therapies used in real practice. The study has an ambispective design with two main visits. At the first visit, physicians will collect baseline data from the past 52 weeks using medical records and patient interviews. The second visit, conducted 12 weeks later, will gather follow-up information on treatment changes and clinical outcomes. A subgroup of 500 patients using fixed-dose combination budesonide/salbutamol will have an additional third visit 12 weeks after the second to collect further data. Participants will undergo routine clinical assessments during 2 to 3 visits following standard practice. Researchers will examine demographic and clinical data, blood and sputum eosinophil counts, total IgE levels, asthma control status, lung function tests, exacerbation rates, and healthcare resource use. Safety monitoring aligns with routine care, and the study does not involve any experimental treatments or procedures. Total participation spans approximately 24 weeks for those in the extended follow-up group.

CONDITIONS

Brief Title

Clinical& Demographic Profiles of patIents With unControllEd Asthma in Russia: Multi-center oBsErvational ReGistry Study

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older at the time of inclusion
  • Signed and dated informed consent prior to study participation
  • Diagnosis of uncontrolled mild or moderate asthma according to GINA score
  • Availability of at least 52 weeks of follow-up data in medical records prior to inclusion
Not Eligible

You will not qualify if you...

  • Severe asthma or current/previous biological therapy within the past 52 weeks
  • Current or past diagnosis of chronic obstructive pulmonary disease (COPD) or idiopathic pulmonary fibrosis (ILF)
  • Participation in any clinical study currently or within the last 52 weeks
  • Any acute or chronic disease that limits study participation or affects results interpretation as judged by the investigator

AI-Screening

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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)

Monitoring

Duration - Retrospective 52 weeks prior to inclusion

Participants' baseline demographic and clinical data from the previous 52 weeks are collected based on medical records and interviews during routine clinical visits.

1 baseline visit (in-person)

Surveillance

Duration - 12 weeks (±7 days)

Participants are observed during routine clinical practice to collect follow-up data on treatment changes and clinical outcomes of uncontrolled asthma.

1 follow-up visit (in-person)

Long-term Monitoring

Duration - Additional 12 weeks (±14 days) after the previous follow-up

For participants receiving fixed-dose combination budesonide/salbutamol, an additional follow-up occurs to collect further data on treatment and clinical outcomes during routine care.

1 additional follow-up visit (in-person)

Trial Site Locations

Total: 47 locations

1

Research Site

Astrakhan, Russia

Actively Recruiting

2

Research Site

Blagoveshchensk, Russia

Active, Not Recruiting

3

Research Site

Bryansk, Russia

Actively Recruiting

4

Research Site

Chelyabinsk, Russia

Actively Recruiting

5

Research Site

Gatchina, Russia

Actively Recruiting

6

Research Site

Irkutsk, Russia

Actively Recruiting

7

Research Site

Ivanovo, Russia

Actively Recruiting

8

Research Site

Izhevsk, Russia

Actively Recruiting

9

Research Site

Kazan', Russia

Actively Recruiting

10

Research Site

Kemerovo, Russia

Actively Recruiting

11

Research Site

Krasnodar, Russia

Actively Recruiting

12

Research Site

Krasnoyarsk, Russia

Actively Recruiting

13

Research Site

Lipetsk, Russia

Actively Recruiting

14

Research Site

Makhachkala, Russia

Actively Recruiting

15

Research Site

Moscow, Russia

Actively Recruiting

16

Research Site

Murmansk, Russia

Actively Recruiting

17

Research Site

Nal'chik, Russia

Actively Recruiting

18

Research Site

Nizhny Novgorod, Russia

Active, Not Recruiting

19

Research Site

Nizhny Tagil, Russia

Actively Recruiting

20

Research Site

Novokuznetsk, Russia

Actively Recruiting

21

Research Site

Novosibirsk, Russia

Actively Recruiting

22

Research Site

Omsk, Russia

Actively Recruiting

23

Research Site

Omsk, Russia

Active, Not Recruiting

24

Research Site

Orenburg, Russia

Actively Recruiting

25

Research Site

Perm, Russia

Actively Recruiting

26

Research Site

Petrozavodsk, Russia

Actively Recruiting

27

Research Site

Pyatigorsk, Russia

Actively Recruiting

28

Research Site

Rostov-on-Don, Russia

Actively Recruiting

29

Research Site

Ryazan, Russia

Actively Recruiting

30

Research Site

Saint Petersburg, Russia

Actively Recruiting

31

Research Site

Saint Petersburg, Russia

Active, Not Recruiting

32

Research Site

Samara, Russia

Actively Recruiting

33

Research Site

Saratov, Russia

Actively Recruiting

34

Research Site

Smolensk, Russia

Withdrawn

35

Research Site

Stavropol, Russia

Actively Recruiting

36

Research Site

Surgut, Russia

Actively Recruiting

37

Research Site

Tomsk, Russia

Actively Recruiting

38

Research Site

Tula, Russia

Actively Recruiting

39

Research Site

Ufa, Russia

Actively Recruiting

40

Research Site

Ulan-Ude, Russia

Actively Recruiting

41

Research Site

Verkhnyaya Pyshma, Russia

Actively Recruiting

42

Research Site

Vladimir, Russia

Actively Recruiting

43

Research Site

Vladivostok, Russia

Actively Recruiting

44

Research Site

Voronezh, Russia

Actively Recruiting

45

Research Site

Yaroslavl, Russia

Actively Recruiting

46

Research Site

Yekaterinburg, Russia

Actively Recruiting

47

Research Site

Yuzhno-Sakhalinsk, Russia

Actively Recruiting

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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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