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Efficacy and Safety of Ganyushu Granule in Treatment of Premenstrual Syndrome with Gan(Liver)Depression and Qi Stagnation Syndrome:A Randomized,Double-Blind,Multicenter,Phase-ⅡClinical Trial
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作者 TENG Xiu-xiang XU Lian-wei +7 位作者 LIN Jie ZHANG Jin-feng ZHANG Qin SUN Yun YANG De-feng LI Hong-mei ZHAO Pei LIU Jun 《Chinese Journal of Integrative Medicine》 SCIE CAS CSCD 2024年第9期771-779,共9页
Objective:To confirm the efficacy and safety of Ganyushu Granule(GYSG)in treating premenstrual syndrome(PMS)in patients with Gan(Liver)depression and qi stagnation syndrome(GDQSS)and determine its effective dosage.Met... Objective:To confirm the efficacy and safety of Ganyushu Granule(GYSG)in treating premenstrual syndrome(PMS)in patients with Gan(Liver)depression and qi stagnation syndrome(GDQSS)and determine its effective dosage.Methods:From June 2018 to March 2021,a total of 240 PMS women with GDQSS were included and randomly divided into 3 groups in a 1:1:1 ratio using central block randomization:high-dose GYSG group(n=78,GYSG 2 packs/time),low-dose GYSG group(n=82,GYSG and its simulant 1 pack/time),and placebo group(n=80,GYSG simulant 2 packs/time).Treatment with GYSG or placebo was given thrice daily and for up to 3 menstrual cycles.Primary outcomes were PMS diary(PMSD)score and premenstrual tension syndrome self-rating scale(PMTS).Secondary outcomes were Chinese medicine(CM)syndrome efficacy.PMSD,PMTS,and efficacy of CM were evaluated with menstrual cycles during the treatment period.Outcome indicators were analyzed after each menstrual cycle.All analyses were performed using an intention-to-treat method,and clinical safety was assessed.Results:Of the 216 patients included in the effectiveness analysis,70,75,and 71 patients were in the high-,low-dose GYSG,and placebo groups,respectively.From the 2nd treatment cycle,the change in PMSD scores in the high-and low-dose groups was lower than that in the placebo group(P<0.05).PMTS scores in the high-dose GYSG group after the 1st treatment cycle was lower than that in the placebo group(P<0.05),while after the 3rd treatment cycle,that in the low-dose group was lower than that in the placebo group(P<0.05).After the 2nd treatment cycle,the high-dose GYSG group had the best CM syndrome efficacy(P<0.05).No serious adverse reactions were reported.Conclusions:GYSG was safe and well-tolerated at both doses for treating PMS patients with GDQSS.High-dose GYSG might be the optimal dose for a phaseⅢtrial. 展开更多
关键词 premenstrual syndrome Chinese medicine ganyushu Granule randomized controlled trial
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肝郁舒颗粒挥发油包合工艺的研究 被引量:1
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作者 单玉荣 《安徽医药》 CAS 2010年第11期1274-1276,共3页
目的优选肝郁舒颗粒的挥发油包合工艺条件。方法采用饱和水溶液法制备包合物,用正交试验,以挥发油包合率和包合物收得率为指标,优选挥发油包合工艺条件。结果最佳工艺为:β-CD∶油(6∶1),包合温度45℃,包合时间2 h。结论此工艺包合效率... 目的优选肝郁舒颗粒的挥发油包合工艺条件。方法采用饱和水溶液法制备包合物,用正交试验,以挥发油包合率和包合物收得率为指标,优选挥发油包合工艺条件。结果最佳工艺为:β-CD∶油(6∶1),包合温度45℃,包合时间2 h。结论此工艺包合效率高,稳定性好,适合工业化生产。 展开更多
关键词 肝郁舒颗粒 挥发油 包合工艺 正交试验
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肝郁舒颗粒质量标准的研究 被引量:4
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作者 颜晓航 金斌 《药物分析杂志》 CAS CSCD 北大核心 2006年第9期1274-1277,共4页
目的:建立肝郁舒颗粒的质量标准。方法:采用TLC法鉴别方中柴胡、白芍、枸杞子、枳壳、佛手;用HPLC法测定白芍中芍药苷的含量。结果:在TLC色谱中可检出柴胡、白芍、枸杞子、枳壳、佛手的特征斑点;芍药苷平均加样回收率为99.71%,RSD为1.6... 目的:建立肝郁舒颗粒的质量标准。方法:采用TLC法鉴别方中柴胡、白芍、枸杞子、枳壳、佛手;用HPLC法测定白芍中芍药苷的含量。结果:在TLC色谱中可检出柴胡、白芍、枸杞子、枳壳、佛手的特征斑点;芍药苷平均加样回收率为99.71%,RSD为1.6%。结论:所建鉴别方法专属性强,定量方法简便、准确。能有效地控制制剂的质量。 展开更多
关键词 肝郁舒颗粒 TLC HPLC 芍药苷
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