Exploring the Efficacy of the Traditional Chinese Medicine Compound Formulas Qianlong Shutong Formula in the Treatment of Benign Prostatic Hyperplasia

Ze-Chao Zhang, Shuping Huang, Changjie Shang, Zesen Lin, Qinyun Yang, Fang Hu, Min Zhu
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Abstract

Objective: This study aimed to assess the efficacy of the compound formula Qianlong Shutong Formula (QLSTF) in the treatment of benign prostatic hyperplasia (BPH) and its impact on hepatic and renal function. This assessment was conducted through randomized controlled trials and animal experimentation. Methods: A total of 160 BPH patients aged between 50 and 70 years were randomly allocated into two groups: The tamsulosin hydrochloride sustained-release capsules group (n=80) and the QLSTF + tamsulosin hydrochloride sustained-release capsules group (n=80). Both groups received a 12-week treatment regimen. In the animal experiments, 12 Sprague Dawley rats were categorized into three groups: The control group (n=4), the model group (n=4), and the QLSTF group (n=4). The latter group received herbal treatment for a duration of 28 days. Results: The current results showed, substantial improvements were observed in the clinical symptoms and signs of BPH within both drug groups. Additionally, no adverse effects on hepatic or renal function were detected. The QLSTF group exhibited a total effective rate of 90.41%, while the control group recorded 77.33%. During the course of treatment, three patients experienced dizziness, and two patients reported nausea and reduced appetite. However, these adverse reactions subsided after a rest period of 4-6h. Conclusion: Our findings underscore the advantages and safety of orally administered QLSTF. In the treatment of BPH, the combined treatment approach using QLSTF demonstrated a higher clinical efficacy rate when compared to the use of tamsulosin hydrochloride sustained-release capsules alone.
中药复方乾隆舒通方治疗良性前列腺增生症的疗效探讨
研究目的本研究旨在评估复方千龙舒通方(QLSTF)治疗良性前列腺增生症(BPH)的疗效及其对肝肾功能的影响。该评估通过随机对照试验和动物实验进行。研究方法将年龄在 50 至 70 岁之间的 160 名良性前列腺增生症患者随机分为两组:盐酸坦索罗辛缓释胶囊组(n=80)和 QLSTF + 盐酸坦索罗辛缓释胶囊组(n=80)。两组均接受为期 12 周的治疗。在动物实验中,12 只 Sprague Dawley 大鼠被分为三组:对照组(4 只)、模型组(4 只)和 QLSTF 组(4 只)。模型组接受为期 28 天的草药治疗。结果显示目前的结果显示,两组药物均能显著改善良性前列腺增生症的临床症状和体征。此外,未发现对肝肾功能的不良影响。QLSTF 组的总有效率为 90.41%,而对照组为 77.33%。在治疗过程中,3 名患者出现头晕,2 名患者出现恶心和食欲下降。不过,在休息 4-6 小时后,这些不良反应均有所缓解。结论我们的研究结果凸显了口服 QLSTF 的优势和安全性。在治疗良性前列腺增生症方面,与单独使用盐酸坦索罗辛缓释胶囊相比,使用 QLSTF 的联合治疗方法显示出更高的临床有效率。
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