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首页> 外文期刊>International journal of gynecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics >Randomized double‐blind placebo‐controlled trial of the effect of Morus nigra Morus nigra L. (black mulberry) leaf powder on symptoms and quality of life among climacteric women
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Randomized double‐blind placebo‐controlled trial of the effect of Morus nigra Morus nigra L. (black mulberry) leaf powder on symptoms and quality of life among climacteric women

机译:随机的双盲安慰剂对照试验Morus nigra Morus nigra L.(黑桑树)叶粉对血小妇女性症状和生活质量的影响

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Abstract Objective To test the efficacy of Morus nigra L . ( MN ) leaf powder for treating climacteric symptoms by comparison with hormone therapy ( HT ) and placebo. Methods A randomized controlled trial among 62 climacteric women attending Hospital of the Federal University of Maranh?o, Brazil. Women were divided into MN , HT , and placebo groups, and received 250?mg of MN leaf powder, 1?mg of estradiol, or placebo for 60?days. Primary outcomes were the Blatt–Kupperman index ( BKI ) for climacteric symptoms and SF ‐36 health questionnaire scores. Results Baseline sociodemographic variables, BKI scores, symptoms, and SF ‐36 domains did not differ among the groups. There was a reduction in mean BKI in the MN (17.5 vs 9.7, P 0.001), HT (15.4 vs 8.6, P =0.001), and placebo (16.1 vs 12.4, P =0.040) groups. Analysis of quality of life (QoL) showed that functional capacity ( P =0.006), vitality ( P =0.031), mental health ( P =0.017), and social aspect ( P 0.01) improved after treatment in the MN group. The HT group showed improvement in emotional limitation ( P =0.040), and the placebo group showed better functional capacity ( P =0.030) after treatment. Conclusions Climacteric symptoms and QoL improved after administration of 250?mg of MN leaf powder for 60?days, similar to the effects of HT . The trial is registered in the Brazilian Registry of Clinical Trials ( REBEC ) under registration number RBR ‐9t4xxk.
机译:摘要目的是测试Morus nigra l的疗效。 (Mn)叶粉通过与激素治疗(HT)和安慰剂进行比较治疗更年性症状。方法采用62名中医大学玛拉尼大学医院的随机对照试验吗?o,巴西。妇女分为Mn,HT和安慰剂组,并接受250毫克MN叶粉,1?Mg雌二醇,或安慰剂60?天。主要结果是用于中生症状的Blatt-Kupperman指数(BKI)和SF -36健康问卷评分。结果基线基线社会阶段变量,BKI评分,症状和SF -36域在组中没有差异。在Mn中的平均BKI(17.5 Vs 9.7,P <0.001),HT(15.4 Vs 8.6,P = 0.001),和安慰剂(16.1 vs 12.4,p = 0.040)组。寿命质量分析(QOL)表明功​​能能力(P = 0.006),活力(P = 0.031),心理健康(P = 0.017)和在Mn组中治疗后改善的社会方面(P <0.01)。 HT组显示出情绪限制的改善(P = 0.040),安慰剂组在处理后显示出更好的功能能力(P = 0.030)。结论将施用250μmmn叶粉60?天,类似于HT的效果后改善了更新症状和QOL。该试验在注册号RBR -9T4XXK下的临床试验(Rebec)的巴西登记处注册。

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