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Data Collection on Treatment Patterns and Clinical Outcomes of Allergic Rhinitis in the Real-World Setting in China

Data Collection on Treatment Patterns and Clinical Outcomes of Allergic Rhinitis in the Real-World Setting in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124146
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-30
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Allergic rhinitis

Interventions

Queue 3(Western medicine + Chinese patent medicine (mainly including Yiqi Tongqiao Pills)):None
Queue 1(Western medicine * (such as antihistamines, nasal hormones, etc.)):None
Queue 2(Chinese patent medicines (mainly including Yiqi Tongqiao Pills)):None

Sponsors

Jiangsu Province Hospital (The First Affiliated Hospital with Nanjing Medical University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age 18 years old and above, gender not limited; 2.Diagnosed by a clinical doctor as allergic rhinitis; 3.One or more allergens tested positive (such as pollen, fungi, etc.), with a positive result for skin prick test (2+ or above), or a positive result for any allergen in the serum allergen test (results from the past 12 months are acceptable); 4.The clinical doctor prescribes Western medicine or Chinese patent medicine prescriptions based on their usual clinical practice for treatment. 5.Voluntary signing of the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with nasal polyps, acute sinusitis, upper respiratory tract infection, nasal tumors, and severe deviation of the nasal septum will be included; 2.Severe heart and lung diseases, serious blood system disorders, or other severe diseases that threaten the patient's life, such as malignant tumors, etc; 3.Those who are allergic to the drug ingredients/formulation; 4.Have been participating in other interventional clinical studies within the past three months; 5.The researchers considered themselves ineligible to participate in this study.

Design outcomes

Primary

MeasureTime frame
Overall Effectiveness;

Secondary

MeasureTime frame
Total nasal symptom score (TNSS) score;Visual analogue scale (VAS);

Countries

China

Contacts

Public ContactCheng Lei

Jiangsu Province Hospital (The First Affiliated Hospital with Nanjing Medical University)

chenglei@jsph.org.cn+86 13776620807

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026