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临床试验/ACTRN12615000794505
ACTRN12615000794505已完成4 期

In persons receiving treatment with zoledronic acid for fracture prevention or Paget's disease, does the administration of oral dexamethasone, compared to placebo, reduce the incidence of acute phase response?

Bone & Joint Research Group, University of Auckland0 个研究点目标入组 40 人开始时间: 2015年7月30日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
20 Years 至 o limit(—)
性别
All

入选标准

  • Females or males aged 20 or older.
  • Prescribed zoledronic acid for the first time for fracture prevention or Paget's disease.

排除标准

  • Prior treatment with zoledronic acid.
  • History of fever, infection, or influenza-like illness within the past week.
  • Diabetes mellitus or uncontrolled hypertension (BP >160/90)
  • Treatment with glucocorticoids within the past week.
  • History of adverse reaction to glucocorticoids.
  • Major systemic illness, including malignancy.

研究者

发起方
Bone & Joint Research Group, University of Auckland

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