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

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单位: [1]Fudan Univ, Shanghai Hua Dong Hosp, Ctr Osteoporosis, Shanghai 200433, Peoples R China [2]Shanghai Jiao Tong Univ, People Hosp 9, Dept Orthoped, Shanghai 200030, Peoples R China [3]Jilin Univ, Dept Orthoped, Hosp 1, Changchun 130023, Ji Lin Province, Peoples R China [4]Capital Med Univ, Beijing Sino Japan Friendship Hosp, Beijing, Peoples R China [5]Chinese Univ Hong Kong, Dept Orthopaed & Traumatol, Hong Kong, Hong Kong, Peoples R China [6]INSERM, Res Unit 664, F-69008 Lyon, France [7]Synarc Clin Res Ctr, San Francisco, CA USA [8]Ji Nan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou, Guangdong, Peoples R China [9]Chinese Acad Sci, Translat Med Res & Dev Ctr, Inst Biomed & Hlth Engn, Shenzhen Inst Adv Technol, Shenzhen, Peoples R China [10]Synarc Clin Res Ctr, Stanford, CA 94305 USA [11]Synarc Biochem Marker Div, Lyon, France
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关键词: Chinese herb Clinical trial Osteoporosis

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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 similar to aEuro parts per thousand 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 (a parts per thousand yen60 years old) with BMD T-score a parts per thousand currency signaEuro parts per thousand a'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 < 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. 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.

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出版当年[2011]版:
大类 | 2 区 医学
小类 | 2 区 内分泌学与代谢
最新[2025]版:
大类 | 2 区 医学
小类 | 2 区 内分泌学与代谢
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出版当年[2010]版:
Q1 ENDOCRINOLOGY & METABOLISM
最新[2024]版:
Q1 ENDOCRINOLOGY & METABOLISM

影响因子: 最新[2024版] 最新五年平均[2021-2025] 出版当年[2010版] 出版当年五年平均[2006-2010] 出版前一年[2009版] 出版后一年[2011版]

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第一作者单位: [1]Fudan Univ, Shanghai Hua Dong Hosp, Ctr Osteoporosis, Shanghai 200433, Peoples R China
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