跳至主要内容
临床试验/NCT03702140
NCT03702140招募中2 期

Examination How the Administration Period of Teriparatide Affects Bone Metabolism and Bone Mineral Density Prior to Denosumab Therapy

Shinshu University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2018年10月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
90
试验地点
1
主要终点
Bone mineral density

研究概览

简要总结

The aim of this study is to examine the efficacy and adverse events in the following 3 groups in osteoporosis patients:

  1. The administration period of teriparatide is less than 6 months and thereafter, denosumab for 24 months.
  2. The administration period of teriparatide is from 6 to 12 months and thereafter, denosumab for 24 months.
  3. The administration period of teriparatide is more than 12 months and thereafter, denosumab for 24 months.

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
Single (Participant)

入排标准

年龄范围
20 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Osteoporotic patients who want to take teriparatide and denosumab

排除标准

  • Patients who are allergic to teriparatide or denosumab Patients who are pregnant or breast-feedin

研究组 & 干预措施

TPTD 6M

Active Comparator

干预措施: "Teriparatide", "Forteo® or Teribon" (Drug)

TPTD 6-12M

Active Comparator

干预措施: "Teriparatide", "Forteo® or Teribon" (Drug)

TPTD 12-24M

Active Comparator

干预措施: "Teriparatide", "Forteo® or Teribon" (Drug)

结局指标

主要结局

Bone mineral density

时间窗: Change from Baseline Values at 1 year

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yukio Nakamura

Lecturer at Shinshu University School of Medicine

Shinshu University

研究点 (1)

Loading locations...

相似试验