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Evaluating Yupingfeng Nasal Drops for Allergic Rhinitis: A Clinical Study

Clinical Observation of Yupingfeng Nasal Drops in the Treatment of Allergic Rhinitis with Lung-Spleen Qi Deficiency Pattern

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000989
Enrollment
Unknown
Registered
2025-05-15
Start date
2024-07-02
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Allergic rhinitis

Interventions

Sham group:10% Yu-Ping-Feng Nasal Spray
Experimental group:Yu-Ping-Feng Nasal Spray

Sponsors

Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria of both traditional Chinese and Western medicine; (2) Aged between 18 and 65 years regardless of gender; (3) Have not received any medication for AR in the past two weeks; (4) Have normal cognitive function agree to voluntarily participate in this trial and sign the informed consent form; (5) All patients and accompanying family members are aware of and understand the purpose significance and process of this research project.

Exclusion criteria

Exclusion criteria: (1) Patients who do not meet the diagnostic or inclusion criteria; (2) Patients with severe nasal septum deviation chronic rhinosinusitis bronchial asthma nasal polyps or other related diseases; (3) Patients with severe dysfunction of the heart liver kidneys or other organs or those with autoimmune diseases; (4) Patients with mental illness intellectual disabilities or other conditions that prevent them from cooperating with the trial; (5) Patients who are pregnant breastfeeding or planning to conceive; (6) Patients with major neurological or psychiatric disorders that prevent them from taking medication regularly; (7) Patients with known allergies to any component of the investigational drug; (8) Patients who have participated in other clinical studies within the past two months.

Design outcomes

Primary

MeasureTime frame
Nasal symptom score;

Secondary

MeasureTime frame
TCM Syndrome score;Transforming growth factor beta 1;Symptom score;Rhinoconjunctivitis quality of life scale;Interleukin 10;Interleukin 17;

Countries

China

Contacts

Public ContactLi Tian

Hospital of Chengdu University of Traditional Chinese Medicine

18980880129@qq.com18980880129

Outcome results

None listed

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