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A machine learning of the duration of omalizumab treatment efficacy for allergic rhinitis

A machine learning of the duration of omalizumab treatment efficacy for allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112034
Enrollment
Unknown
Registered
2025-11-10
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

allergic rhinitis

Interventions

Research group:None

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients meet the clinical diagnostic criteria of the latest allergic rhinitis treatment guidelines; 2. Subjects test positive for allergens: allergen-specific IgE or total serum IgE is positive, and allergen skin prick test is positive; 3. Patients with moderate to severe perennial allergic rhinitis whose symptoms cannot be adequately controlled by standardized symptomatic medication; 4. Patients receiving anti-IgE monoclonal antibody therapy and have signed the informed consent for this treatment plan.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to the active ingredient of Omalizumab or other excipients; 2. Patients with acute attacks or acute exacerbation of asthma complicated by allergic rhinitis; 3. Patients at high risk of parasitic infections such as worms; 4. Patients with severe systemic diseases (such as immunodeficiency or malignant tumors); 5. Patients with acute infections; 6. Patients lost to follow-up.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;Total Nasal Symptom Score;

Countries

China

Contacts

Public ContactYuqin Deng

Renmin Hospital of Wuhan University

bamboo0723@126.com+86 27 88041911

Outcome results

None listed

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