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Bencycloquidium bromide nasal spray is effective and safe for persistent allergic rhinitis: a phase III, multicenter, randomized, double-blinded, placebo-controlled clinical trial

鼻漏 鼻塞 医学 鼻孔 可视模拟标度 瘙痒的 鼻喷雾剂 安慰剂 安慰剂组 鼻腔给药 随机对照试验 外科 麻醉 不利影响 内科学 鼻子 免疫学 替代医学 病理
作者
Zihan Jiang,Hao Xiao,Shixi Liu,Gang He,Guo‐Hua Hu,Xueyuan Zhang,Qinna Zhang,Jichuan Chen,Chang Sheng Lin,Jianping Liang,Mingli Guo,Xuping Xiao,Wei-guo Xue,Pin Dong,Yongwang Huang,Zhuang Lian,Guolin Tan,Jia He,Yuanyuan Pan,Juan Meng
出处
期刊:European Archives of Oto-rhino-laryngology [Springer Science+Business Media]
卷期号:277 (11): 3067-3077 被引量:13
标识
DOI:10.1007/s00405-020-06183-5
摘要

To investigate the efficacy and safety of bencycloquidium bromide nasal spray (BCQB) in patients with persistent allergic rhinitis (PAR). We enrolled 720 patients from 15 hospitals across China and randomly assigned them into BCQB group or placebo group (90 μg per nostril qid) to receive a 4-week treatment. Visual analog scale (VAS) for rhinorrhea, sneezing, nasal congestion, itching and overall symptoms were recorded by patients every day. Anterior rhinoscopy scoring was completed by doctors on every visit. Adverse events were recorded in detail. A total of 354 and 351 patients were included in BCQB group and in placebo group. Baseline information was comparable. At the end of the trial, the decrease of VAS for rhinorrhea from baseline was 4.83 ± 2.35 and 2.46 ± 2.34 in BCQB group and placebo group, respectively (P < 0.001). The change ratio from baseline of VAS for rhinorrhea in BCQB group was 72.32%, higher than 31.03% in placebo group (P < 0.001). VAS for other symptoms and overall symptoms also improved significantly in the BCQB group, while no inter-group difference was found in anterior rhinoscopy scoring. The incidence of adverse reaction was similar between the two groups. Most reactions were mild and no severe reactions happened. 90 μg BCQB per nostril four times daily is effective and safe in the treatment of rhinorrhea as well as sneezing, nasal congestion and itching for patients with PAR. ChiCTR2000030924, 2020/3/17.
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