Skip to content

The clinical efficacy evaluation after house dust mite specific subcutaneous immunotherapy for three years

Five-year fellow-up clinical efficacy evaluation after house dust mite specific subcutaneous immunotherapy for three years in patients with asthma and/or allergic rhinitis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15006207
Enrollment
Unknown
Registered
2015-04-07
Start date
2015-04-01
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

Allergy

Interventions

children:Nil
Adult:Nil

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Written informed consent obtained before entering the trial; 2. Male or female to be aged 5 to 55 years old; 3. Have accepted house dust mite specific subcutaneous immunotherapy for 3 years,and the discontinued treatment period was not over 6 months; 4. With good compliance.

Exclusion criteria

Exclusion criteria: 1. Participate in other clinical drug trials in 3 months; 2. A clinical history of COPD; 3. More than 10 pack years of smoking history; 4. Any of the following underlying conditions known or suspected to be present: Cystic fibrosis, malignancy, insulin-dependent diabetes, malabsorption or malnutrition, renal, or hepatic insufficiency, chronic infection or with any evidence of disease making implementation of the protocol or interpretation of the protocol results difficult or jeopardising the safety of the patient (e.g. clinically significant cardiovascular, serious immunopathologic, immunodeficiency whether acquired or not, hepatic, neurologic, psychiatric, endocrine, or other major systemic disease); 5. History in the previous 4 weeks of exacerbations of asthma(systemic corticosteroids use for asthma or need for emergency or hospitalization.

Design outcomes

Primary

MeasureTime frame
symptom score and drug score;specific IgE;specific IgG4;T-reg cell;

Countries

China

Contacts

Public ContactJing Li
lijing@gird.cn+86 020-34296151

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026