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A study on predicting the efficacy of allergen-specific immunotherapy for mite allergic rhinitis in children

A study on predicting the efficacy of allergen-specific immunotherapy for mite allergic rhinitis in children

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072847
Enrollment
Unknown
Registered
2023-06-27
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Alllergic rhinitis

Interventions

Experimental group:Allergen immunotherapy

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years

Inclusion criteria

Inclusion criteria: ? In line with the "Guidelines for the Diagnosis and Treatment of Allergic Rhinitis (2015)" guidelines for the diagnosis of allergic rhinitis. ? Age: 5-12 years old (gender is not limited) ? Serum house dust mite/dust mite specific IgE = 0.35 or mite allergen skin test =++. ? In line with ARIA guidelines for allergen-specific immunotherapy indications and no contraindications. ? Agree to carry out nasal allergen challenge test and nasal secretion collection. ? The parents/legal guardians of the children must sign the informed consent form for the children to participate in this study.

Exclusion criteria

Exclusion criteria: A "yes" result for any of the following criteria will not be eligible for selection. ? Received allergen-specific immunotherapy in the past. ? Received treatment with systemic glucocorticoids, omalizumab, dupilimumab and other biological agents in the past 6 months. ? Combined with chronic sinusitis/nasal polyps (examination based on clinical history, electronic nasal endoscopy and/or sinus CT examination if necessary). ? Dust mites are not major allergens. ? Those who are currently at the onset of diseases such as upper respiratory tract infection, acute sinusitis, acute otitis media or other related infectious diseases or are receiving treatment. ? Diagnosis of heart, lung, liver, kidney, blood and other basic diseases. ? Those who are receiving beta-blocker therapy. ? Those who have allergies, hypersensitivity reactions or intolerance to emergency medicines. ? Mentally disabled, unable to understand the nature, significance and expected consequences of the research, and/or uncooperative attitude.

Design outcomes

Primary

MeasureTime frame
VAS score;TNSS;Proteomics of nasal secretions;

Secondary

MeasureTime frame
Serum proteomics;Dust mite allergen components;

Countries

China

Contacts

Public ContactBaoqing Sun

The First Affiliated Hospital of Guangzhou Medical University

hustgh@hotmail.com+86 189 2886 8236

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026