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A cohort study of Huaiqihuang Granules Combined with nasal glucocorticoids in the treatment of allergic rhinitis in children

A cohort study of Huaiqihuang Granules Combined with nasal glucocorticoids in the treatment of allergic rhinitis in children

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102034
Enrollment
Unknown
Registered
2025-05-07
Start date
2025-05-07
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Allergic rhinitis in children

Interventions

Combination therapy group:Huaiqihuang granules combined with a nasal corticosteroid preparation for the treatment of allergic rhinitis with a course of treatment of >=4 weeks
Control group:Patients with allergic rhinitis treated with nasal corticosteroid preparations for a duration of >= 4 weeks

Sponsors

Chengdu Women's and Children's Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: Children who meets the diagnostic criteria for allergic rhinitis according to the child's family history and typical allergy history, clinical manifestations, and a series of laboratory tests ; age range 2 to 12 years old; Point prick test found >= 1 allergen; Obtained the right to informed consent from the guardian; Patients who receive nasal corticosteroid preparations in their medication treatment plan and have a treatment duration of >= 4 weeks; The combination therapy group must meet the following requirements: the drug treatment plan includes both nasal corticosteroid preparations and Huaiqihuang granules, and the combination therapy course is >= 4 weeks.

Exclusion criteria

Exclusion criteria: Patients has other comorbidities; Have undergone relevant disease surgeries before the study; Individuals who are allergic to the drugs used in this study; Those who cannot follow the rules of medical advice for treatment; After inclusion, it was found that the product did not meet the requirements and was mistakenly accepted; Not treated as required; Unable to conduct data collection and efficacy evaluation normally; Those who have poor medication adherence and continue treatment after treatment interruption; Those who have not undergone relevant symptom scoring and immune index testing.

Design outcomes

Primary

MeasureTime frame
Response rate;Recurrence rate;

Countries

China

Contacts

Public ContactYi Deng

Chengdu Women's and Children's Central Hospital

9306179@qq.com+86 130 1827 3737

Outcome results

None listed

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