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Investigate the indoor allergen exposure and evaluate the efficacy of allergy immunotherapy on allergic rhinitis and/or asthma children

Investigate the indoor allergen exposure and evaluate the efficacy of allergy immunotherapy on allergic rhinitis and/or asthma children

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15006105
Enrollment
Unknown
Registered
2015-02-10
Start date
2008-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

House dust mite induced allergic asthma/rhinitis

Interventions

treatment:immunotherapy
control:symptomatic drug

Sponsors

Nanjing Children's hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1. Age 5-14year (No gender preference); 2. Mild to moderate allergic rhinitis (or with allergic athma)patient, PEF>=70%of predicted value; 3. Positive Skin Prick Test (SPT) response, wheal SI index >=0.5(++); 4. Patients who is fail to meet one of the above criteria is excluded from the trial.

Exclusion criteria

Exclusion criteria: 1. EFV1 <=70% of predicted value; 2. Asthma onset during the screen period, accept the treatment of inhaled or systematic corticosteroids, the daily dose over 800ug of Beclomethasone, over 15 days, or take oral prednisone frequently; 3. Current upper respiratory tract infection, severe atopic dermatitis, acute sinusitis, acute ear or other relevant infectious diseases or under the treatment; 4. Previous treatment by immunotherapy with house dust mite allergen extracts within the previous 5 years; 5. With underlying diseases such as heart disease, pulmonary disease, liver disease, kidney disease and serum diease; 6. Patient is under treatment with beta-blocker; 7. Patient is immune deficiency/low immune function,or under the treatment of immunotherapy; 8. Patient is allergic, hypersensitive or intolerance to first-aid medicine; 9. A mental condition rendering the patient unable to understand the nature, scope and possible consequences of the trial, and/or evidence of an uncooperative attitude; 10. Unlikely to be able to complete the trial, for any reason, or likely to move, or travel for extended periods of time during the trial period; 11. Patients who meet one of above exclusive criteria will be excluded from the trial.

Design outcomes

Primary

MeasureTime frame
Specific IgG4;Specific IgE blocking factor;

Countries

China

Contacts

Public ContactDeyu Zhao
zhaodeyu988@126.com+86 13951896843

Outcome results

None listed

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