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临床试验/NCT00092040
NCT00092040已完成3 期

A Randomized, Double-Blind, Double-Dummy, Parallel-Group, Multicenter Study to Evaluate and Compare the Effects of Alendronate and Risedronate on Bone Mineral Density in Postmenopausal Women With Osteoporosis; A 12 Month Extension to: A Randomized, Double-Blind, Double-Dummy, Parallel-Group, Multicenter Study to Evaluate and Compare the Effects of Alendronate and Risedronate on Bone Mineral Density in Postmenopausal Women With Osteoporosis

Organon and Co0 个研究点目标入组 936 人开始时间: 2003年3月18日最近更新:
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试验速览

阶段
3 期
状态
已完成
入组人数
936
主要终点
Mean percent change from baseline in hip trochanter bone mineral density (BMD)

研究概览

简要总结

The purpose of this study and 12 month extension is to evaluate the effects of two investigational drugs on osteoporosis in postmenopausal women.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Postmenopausal women with osteoporosis

排除标准

  • Any known allergy to the study drug

结局指标

主要结局

Mean percent change from baseline in hip trochanter bone mineral density (BMD)

次要结局

  • Mean percent change from baseline in PA lumbar spine, total hip, and femoral neck BMD

研究者

申办方类型
Industry
责任方
Sponsor

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