【24h】

The first multicenter and randomized clinical trial of herbal Fufang for treatment of postmenopausal osteoporosis.

机译:复方中草药治疗绝经后骨质疏松症的首个多中心随机临床试验。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

This multicenter and randomized clinical trial showed that daily oral herbal formula Xian Ling Gu Bao (XLGB) was safe in postmenopausal women over a 1-year treatment. Those patients (n?~?50) treated with XLGB at the conventional dose demonstrated a statistically significant increase in dual-energy X-ray absorptiometry (DXA) bone mineral density (BMD) at lumbar spine at 6 months and a numerically increased BMD at 12 months.The aim of this study was to examine the safety and efficacy of a herbal formula XLGB in postmenopausal women (ChiCTR-TRC-00000347).One hundred eighty healthy postmenopausal women (≥60 years old) with BMD T-score?≤?-2.0 (lumbar spine or femoral neck) were recruited from four clinical centers to receive low-dose (conventional dose) XLGB (L-XLGB group, 3 g/day, n?=?61) or high-dose XLGB (H-XLGB group, 6 g/day, n?=?58) or placebo (CON group, n?=?61). Women received daily calcium (500 mg) and vitamin D (200 IU) supplementation. Primary endpoints were lumbar spine BMD and safety; secondary endpoints were femoral neck BMD and bone turnover markers measured at baseline and at 6 and 12 months.Of 180 women recruited, 148 completed the study. The compliance in each group was comparable. Prominent adverse events were not observed in either group. In the L-XLGB group at 6 months, lumbar spine BMD by DXA increased significantly from baseline (+2.11% versus CON +0.58%, p?
机译:该多中心随机临床试验表明,每日口服草药配方仙灵骨宝(XLGB)在绝经后妇女中经过1年的治疗是安全的。常规剂量的XLGB治疗的这些患者(n?〜?50)在6个月时腰椎的双能X线骨密度仪(DXA)骨矿物质密度(BMD)显着增加,而BMD在数值上增加。 12个月。这项研究的目的是检查草药配方XLGB在绝经后妇女(ChiCTR-TRC-00000347)中的安全性和有效性。一百八十名健康的绝经后妇女(≥60岁)的BMD T分数≤从四个临床中心招募β-2.0(腰椎或股骨颈)以接受低剂量(常规剂量)XLGB(L-XLGB组,3 g /天,n?=?61)或大剂量XLGB(H -XLGB组,每天6克,n?=?58)或安慰剂(CON组,n?=?61)。妇女每天接受钙(500毫克)和维生素D(200 IU)补充。主要终点为腰椎骨密度和安全性。次要终点是在基线,第6和12个月测量的股骨颈BMD和骨转换指标。在招募的180名妇女中,有148名完成了研究。每个组的依从性是可比较的。两组均未观察到明显的不良事件。 L-XLGB组在6个月时,DXA测得的腰椎BMD与基线相比显着增加(+ 2.11%,而CON + 0.58%,p 0.05),但股骨颈BMD没有升高。在12个月时,L-XLGB组的BMD从6个月的水平下降,但仍高于基线,但与CON组无差异。没有剂量依赖性反应。 XLGB治疗后的最初6个月,骨转换标志物水平下降。在治疗组和对照组之间,总的副作用发生率没有显着差异。以常规剂量治疗1年以上的XLGB证明是安全的,绝经后6个月时腰椎的BMD仅统计上显着增加。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号