uncontrolled asthma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: RCTs that assessed the clinical efficacy and safety of anti-IL-13 therapies in adolescents or adults aged 12 years or older with a diagnosis of uncontrolled, severe, or moderate to severeasthma; and studies whose outcomes included pulmonary function, any adverse event, asthma exacerbation, asthma control, or asthma related quality of life.
Exclusion criteria
Exclusion criteria: Observational, case-control, cohort, and non-blinded clinical trials were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| chenge in FEV1.0 incidence of all adverse events | — |
Secondary
| Measure | Time frame |
|---|---|
| time to first asthma exacerbation change in ACQ score change in AQLQ | — |
Countries
Japan
Contacts
Showa University Division of Respiratory Medicine and Allergology, Department of Medicine