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Evidence-based evaluation research of TCM nasal spray which have the function of replenishing qi and activating blood in the treatment of allergic rhinitis

Efficacy and Safety of Modified Yupingfeng Nasal Spray in Controlling the Recurrence of Persistent and Moderate-Severe Allergic Rhinitis: Study Protocol for a Multicenter, Open-Label, Randomized, and Parallel-Arm Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047053
Enrollment
Unknown
Registered
2021-06-07
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

allergic rhinitis

Interventions

Sponsors

The Teaching 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. Those who meet the above diagnostic standards; 2. Patients with a positive skin prick test of grade 2 or above; 3. Aged 18 to 65 years without gender restriction; 4. Not received any medication for AR in the past two weeks; 5. Agree to participate in this test and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients combined with severe nasal septal deviation, chronic nasal-sinusitis, bronchial asthma, nasal polyps and other diseases; 2. With heart, liver and kidney disorder or autoimmune diseases; 3. combined with mental illness, mental disorders and unable to cooperate to complete the test; 4. Patients during pregnancy, lactation, or during pregnancy preparation; 5. Patient is allergic to the composition of the clinical trial drug; 6. Patients who had received glucocorticoids, leukotriene receptor blockers, antihistamines, or anti-inflammatory drugs within two weeks; 7. Patients with skin pathological changes at the site of the skin prick test; 8. Patients who are currently and have previously participated in specific immunotherapy; 9. Patients who have participated in other clinical studies in the past two months.

Design outcomes

Primary

MeasureTime frame
six-month recurrence rate of AR;

Secondary

MeasureTime frame
Duration of medication (days);Visual analog scale;Rhinoconjunctivitis quality of life scale;Total score for nasal symptoms;Total score for eye symptoms;Chinese Medicine Physique Classification and Judgment Table;Spleen Qi Deficiency Systemic Symptoms Scoring Table;Lung Qi Deficiency Systemic Symptoms Scoring Table;Carbon monoxide;Platelet activating factor;Toll-like receptor 4;Human chemokine receptor 6;Human chemokine receptor 7;Heme oxygenase 1;Myeloid differentiation factor;TIR domain adaptor protein;Interleukin 4;Interferon gamma;Tumor Necrosis Factor Alpha;Nuclear factor-??;Nasal endoscopic results;Rhinitis Control Assessment Test (RCAT);one-month recurrence rate of AR;the duration of follow-up (days);

Countries

China

Contacts

Public ContactTian Li

The Teaching Hospital of Chengdu University of Traditional Chinese Medicine

ctcmdan@stu.cdutcm.edu.cn+86 18980880129

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026