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临床试验/EUCTR2006-004717-17-EE
EUCTR2006-004717-17-EE进行中(未招募)不适用

The efficacy and safety of 2g strontium ranelate in the treatment of osteoporosis in men. A prospective multicentre, international, double-blind, placebo-controlled study with a treatment duration of 2 years and the main study analysis after 1 year.

Institut de Recherches Internationales Servier0 个研究点目标入组 221 人开始时间: 2007年1月11日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
221

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Male

入选标准

  • · The following BMD criterion:
  • Mean lumbar spine BMD or femoral neck BMD or total femur BMD corresponding to a T-score lower than –2.5SD of the young healthy male reference population
  • Mean lumbar spine BMD or femoral neck BMD or total femur BMD corresponding to a T-score lower than –1.5SD of the young healthy male reference population plus a prevalent low impact fracture during adulthood
  • · Caucasian males of at least 65 years of age (with no upper age limit)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • · Bone mineral density T-score below –4.0 at one or more of the measured sites
  • · More than two prevalent mild and/or moderate osteoporotic vertebral fractures
  • · Severe osteoporotic vertebral fracture
  • . Other criteria (detailed in the protocol)

研究者

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