Yupingfeng Powder for Allergic Rhinitis in Adults
Official title: The Effects of Using Yupingfeng Powder With Variation for the Treatment of Allergic Rhinitis (AR): a Randomized Controlled Trial
Run by Chinese University of Hong Kong · NCT06608017 · Data updated 2026-11-12
This study tests whether Yupingfeng Powder, a traditional Chinese herbal medicine, helps adults with allergic rhinitis who have lung and spleen qi deficiency.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 140 (estimated) |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Drugs / interventions | immunotherapy |
| Locations | 1 site (Shatin) |
| Status | Recruiting |
| Started | March 27, 2025 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | July 27, 2026 |
| Trial ID | NCT06608017 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18 or older with allergic rhinitis and evidence of lung and spleen qi deficiency who have at least two nasal symptoms for more than one hour per day.
✕Probably not a fit
Patients without the qi-deficiency profile or those whose symptoms do not respond to the herbal formulation may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional trial investigates the effects of Chinese Herbal Medicine granules (Yupingfeng Powder) versus placebo for adults with allergic rhinitis. It targets patients characterized by lung and spleen qi deficiency and who have multiple symptoms such as runny nose, sneezing, nasal obstruction, or itching for at least one hour daily. The study combines Phase 2 and Phase 3 to evaluate safety and efficacy, using a randomized, blinded design typical of clinical evaluations. Primary outcomes likely include symptom improvement and quality of life, with secondary outcomes addressing safety and tolerability. This trial is conducted at the Hong Kong Institute of Integrative Medicine and is sponsored by The Chinese University of Hong Kong.
Why it matters
Potential benefit: If successful, patients could experience reduced nasal symptoms and improved daily functioning with a traditional medicine approach.
How similar studies have gone: Prior studies in traditional Chinese medicine approaches have shown variable but sometimes favorable results for allergic rhinitis, making this approach plausible but not yet definitive.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Aged 18 or above; * Subjects with deficiency of lung and spleen Qi; * At least 2 or more allergic symptoms (rhinorrhea, sneezing, nasal obstruction and nasal itching) for a cumulative period greater than 1 hour per day; * Understand Chinese; * Voluntary written consent. Exclusion Criteria: * Known chronic disease such as asthma, rhinosinusitis, nasal polyposis; * Known severe medical conditions, such as cardiovascular, liver or renal dysfunction, diabetes mellitus, cancers, cerebrovascular diseases, blood system diseases; * Concomitant steroid, nonsteroidal anti-inflammatory drugs (NSAIDs), anticoagulant, and immunotherapy within past month; * Impaired hematological profile and liver / renal function exceeds the upper limit of the reference value by 2 times ; * Known alcohol and / or drug abuse; * Known allergic history to any Chinese herbal medicines; * Known pregnant or lactating.
Where it's running
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Hong Kong Institute of Integrative Medicine
Shatin, Hong Kong Recruiting
Study contacts
- Principal investigator: Zhixiu Lin, PhD — Chinese University of Hong Kong
- Study coordinator: Zhixiu LIN, PhD
- Email: linzx@cuhk.edu.hk
- Phone: +85235053476
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.