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Observation of clinical outcome of bronchial asthma with allergic rhinitis caused by house dust mite

Observation of clinical outcome of bronchial asthma with allergic rhinitis caused by house dust mite - Treatment for asthma with rhinitis by dust mite

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000026750
Enrollment
60
Registered
2017-03-30
Start date
2016-12-14
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

Bronchial asthma with allergic rhinitis caused by house dust mite

Interventions

None listed

Sponsors

National Hospital Organization Mie National Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Bronchial asthma with allergic rhinitis with disease duration of more than 1 year 2. Sensitization to HDM (specific IgE by ImmunoCAP is greater than or equal to class 2) 3. Positive nasal challenge test to house dust allergen 4. Bronchial asthma as follows; a. Mild to moderate severity, not in acute exacerbation b. FEV1 is greater than or equal to 70% of predicted value c. Reversible respiratory symptoms d. Negative specific IgE (class 0 or 1) to dog, cat, Alternaria, and Aspergillus 5. Be willing to receive medication therapy or allergen immunotherapy for bronchial asthma with allergic rhinitis

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding female 2. Patients with sino-nasal disease that might confound accurate determination of the outcomes of the study 3. Patients with severe asthma 4. Smoker or pet keeper 5. Patients with episode of life-threatening treatment-related adverse event 6. Patients with malignant disease or severe systemic disease which affect immune system 7. Patients who cannot receive sublingual immunotherapy by other reasons

Design outcomes

Primary

MeasureTime frame
Change in symptoms and medication for allergic rhinitis and asthma by treatment with medicine or sublingual immunotherapy for 3 years

Secondary

MeasureTime frame
1. Change in allergic response in nasal mucosa and skin prick test 2. Change in allergic parameters in peripheral blood 3. Compliance of sublingual immunotherapy 4. Safety (adverse event)

Countries

Japan

Contacts

Public ContactSatoko Usui

National Hospital Organization Mie National Hospital Department of Otorhinolaryngology

usuis@mie-m.hosp.go.jp059-232-2531

Outcome results

None listed

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