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临床试验/EUCTR2005-002342-19-CZ
EUCTR2005-002342-19-CZ进行中(未招募)不适用

A multicentre, open label study to evaluate the safety and efficacy of Alendros 70 therapy administered 70mg once a week in women with postmenopausal osteoporosis

Zentiva, a.s.0 个研究点目标入组 100 人开始时间: 2005年6月23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)
发起方
Zentiva, a.s.
入组人数
100

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
Female

入选标准

  • ambulatory,
  • age to 80 years
  • Postmenopausal osteoporosis
  • Meets the BMD criteria of the lumbar spine or proximal femur for osteoporosis
  • Are the trial subjects under 18?
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • 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

  • 1.have evidence of a clinically significant psychiatric or organic disease which could prevent the patient from completing the study
  • 2.abuse of alcohol or use illicit drugs
  • 3.any allergic or abnormal reaction to bisphosphonates
  • 4. hypokalcemia
  • 5. serious disease of the gastrointestinal tract
  • 6. inability be seated for 30 minutes

研究者

发起方
Zentiva, a.s.

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