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

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

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : H. M. Zhu & L. Qin & P. Garnero & H. K. Genant & G. Zhang & K. Dai & X. Yao & G. Gu & Y. Hao & Z. Li & Y. Zhao & W. Li & J. Yang & X. Zhao & D. Shi &
  • چاپ و سال / کشور: 2011

Description

Summary 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. Introduction The aim of this study was to examine the safety and efficacy of a herbal formula XLGB in postmenopausal women (ChiCTR-TRC-00000347). Methods One hundred eighty healthy postmenopausal women (،ف60 years old) with BMD T-score،ـ.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. Results 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<0.05), but femoral neck BMD did not; at 12 months, BMD in the L-XLGB group decreased from 6-month levels yet remained higher than baseline, but without difference from the CON group. There was no dose-dependent response. Bone turnover marker levels declined during the first 6 months after XLGB treatment. There was no significant difference in the overall incidence of side effects among treatment and control groups. Conclusion XLGB over 1-year treatment at the conventional dose demonstrated safe and only a statistically significant increase in BMD at lumbar spine at 6 months in postmenopausal women.
Osteoporos Int DOI 10.1007/s00198-011-1577-2 Received: 29 July 2010 / Accepted: 22 January 2011
اگر شما نسبت به این اثر یا عنوان محق هستید، لطفا از طریق "بخش تماس با ما" با ما تماس بگیرید و برای اطلاعات بیشتر، صفحه قوانین و مقررات را مطالعه نمایید.

دیدگاه کاربران


لطفا در این قسمت فقط نظر شخصی در مورد این عنوان را وارد نمایید و در صورتیکه مشکلی با دانلود یا استفاده از این فایل دارید در صفحه کاربری تیکت ثبت کنید.

بارگزاری