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Preventive immunotherapy for seasonal allergic rhinitis in Inner Mongolia

Preventive immunotherapy for seasonal allergic rhinitis in Inner Mongolia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031810
Enrollment
Unknown
Registered
2020-04-11
Start date
2019-06-04
Completion date
Unknown
Last updated
2020-04-13

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

Conditions

allergic rhinitis

Interventions

Group A:Spleen Aminopeptide Oral Solution
Group B:Spleen Aminopeptide Oral Solution + Loratadine Tablets
Group C:Loratadine Tablets

Sponsors

Affiliated Hospital of Inner Mongolia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years male and female; 2. Criteria for the diagnosis of moderate to severe seasonal AR patients: guidelines for the diagnosis and treatment of allergic rhinitis (2015, tianjin) were formulated; 3. Duration of allergic rhinitis >=2 years; 4. patients sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Non-allergic rhinitis with eosinophilia syndrome; (2) Other types of chronic rhinitis; (3) Accompanied by other serious allergic diseases; (4) Patients with serious heart, liver, kidney and brain diseases; (5) Other conditions in which patients are known or suspected to be unable to adhere to the study protocol or the investigator considers inappropriate for inclusion.

Design outcomes

Primary

MeasureTime frame
Routine blood;Human TH1/TH2 subclass detection;Lymphocyte subsets are absolute;

Countries

China

Contacts

Public ContactCui Xiaobo

Affiliated Hospital of Inner Mongolia Medical University

cxbgh@sina.com+86 18686024380

Outcome results

None listed

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