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        <identifier>oai:figshare.com:article/33985924</identifier>
        <datestamp>2026-09-24T13:55:07Z</datestamp>
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          <dc:title>Supplementary Material for: Efficacy and Safety of Yiqi Tongqiao Pill for Allergic Rhinitis With Lung–Spleen Qi Deficiency: A Multicenter Randomized Double-Blind Phase III Trial</dc:title>
          <dc:creator>figshare admin karger (2628495)</dc:creator>
          <dc:creator>Zhang Y. (2828780)</dc:creator>
          <dc:creator>Liu J. (3215370)</dc:creator>
          <dc:creator>Qiao F. (25104262)</dc:creator>
          <dc:creator>Chen X. (2888087)</dc:creator>
          <dc:creator>Zhu Z. (3610574)</dc:creator>
          <dc:creator>Tao B. (17425752)</dc:creator>
          <dc:creator>Zheng Z. (4158406)</dc:creator>
          <dc:creator>Liu D. (3800659)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:description>OBJECTIVE: To evaluate the clinical efficacy and safety of Yiqi Tongqiao Pill (YQTP) in treating allergic rhinitis (AR) with a Traditional Chinese Medicine (TCM) pattern of Lung-Spleen Qi Deficiency.
METHODS: A multicenter, randomized, double-blind, parallel-controlled, phase III clinical trial was conducted. A total of 480 patients with allergic rhinitis were randomly assigned in a 3:1 ratio to a treatment group (oral YQTP, n=360) and a control group (oral low-dose mimic agent, n=119) for a 2-week course. The primary efficacy endpoint was the change from baseline in the Total Nasal Symptom Score (TNSS) after 2 weeks of treatment.
RESULTS: The Full Analysis Set (FAS) included 479 patients. After 2 weeks of treatment, the reduction in TNSS score in the treatment group (5.79±2.23) was significantly greater than that in the control group (0.84±1.82) (P&lt;0.0001). The treatment group also demonstrated significant superiority over the control group in terms of overall response rate (92.78% vs 10.92%), improvement in TCM syndrome score, quality of life, and speed of symptom relief (all P&lt;0.0001). There was no statistically significant difference in the incidence of adverse events between the two groups, indicating a good safety profile.
CONCLUSION: YQTP significantly improved nasal symptoms and quality of life over 2 weeks in patients with SAR with the TCM pattern of lung–spleen qi deficiency, with a safety profile comparable to the mimic control.
Trial registration: Chinese Clinical Trial Registry (ChiCTR-TRC-13003137); http://www.chictr.org.cn</dc:description>
          <dc:date>2026-09-24T13:55:07Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.33985924.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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