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A non-interventional study to investigate the proportion, characteristics and treatment reality of adult patients with severe and uncontrolled severe asthma using a claims database

A non-interventional study to investigate the proportion, characteristics and treatment reality of adult patients with severe and uncontrolled severe asthma using a claims database - KEIFU study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000027695
Enrollment
20000
Registered
2017-06-14
Start date
2017-07-31
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Interventions

None listed

Sponsors

Astrazeneca K.K
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -17 years of age and older at the index date -Patients who had claim within 12 months prior to Index date -Patients who had a record of asthma diagnosis 12 and more months prior to Index date -Patients who had 4 or more "claims with for an asthma and record of ICS or ICS/LABA prescription for that visit" within 12 months prior to Index date

Exclusion criteria

Exclusion criteria: -Patients who didin't have the "claims with for an asthma and record of ICS or ICS/LABA prescription for that visit" within 6 months prior to Index date -Patients who didin't have the "claims with for an asthma and record of ICS or ICS/LABA prescription for that visit" during the period of more than 6 months and within 12 months prior to Index date

Design outcomes

Primary

MeasureTime frame
Following patient proportion in treated asthma patients; severe asthma, uncontrolled severe asthma

Countries

Japan

Contacts

Public ContactYoko Yoshimura

Astrazeneca K.K Medical department Evidence & Observational Research

yoko.yoshimura@astrazeneca.com06-4802-3600

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026