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A prospective cohort study of omalizumab in the treatment of seasonal allergic rhinitis

A prospective cohort study of omalizumab in the treatment of seasonal allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116867
Enrollment
Unknown
Registered
2026-01-15
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Allergic rhinitis

Interventions

Treatment group:None
Control group:None

Sponsors

Chongqing General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years; 2. Diagnosed with seasonal allergic rhinitis (SAR); 3. Allergen-specific IgE positive (>=3.5 UA/mL); 4. Symptoms are not adequately controlled by conventional therapy (such as antihistamines and nasal steroids); 5. The patient fully understands this study, voluntarily participates, and signs the informed consent form (ICF).

Exclusion criteria

Exclusion criteria: 1. Having other types of rhinitis (such as chronic sinusitis); 2. Having undergone nasal surgery or other immunomodulatory treatment within the past year; 3. Allergy to omalizumab, excipients of the treatment drug, or other biologics, or having a history of severe drug allergy or anaphylactic shock; 4. Having serious cardiovascular, liver, kidney, or other systemic diseases that may affect study results or increase treatment risks; 5. Pregnant or breastfeeding women; 6. Having a history of severe neurological or psychiatric disorders; 7. Patients whom the investigator deems unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Daily Nasal Symptom Score,DNSS;Quality of Life Score;Daily Medication Score;

Countries

China

Contacts

Public ContactDan Zeng

Chongqing General Hospital

zengdan0510@163.com+86 23 43780053

Outcome results

None listed

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