JPRN-UMIN000013014已完成未知
Preventive effects with teriparatide or alendronate on the progression of vertebral collapse - T-WRAP (Teriparatide for new vertebral fractures to wedge deformity prevention study)
Kitakyushu Osteoporosis Trial Unit0 个研究点目标入组 200 人开始时间: 2014年2月1日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- ot applicable 至 ot applicable(—)
- 性别
- Female
入选标准
- 未提供
排除标准
- •1. Patients with vertebral compression fractures which is not clear the time of injury. 2. Patients received teriparatide or denosumab within 6 months prior to the study. 3. Patients with contraindications of teriparatide or alendronate. 4. Patients with severe renal dysfunction, severe liver dysfunction, or severe heart disease. 5. Inappropriate patients to participate the study judged by primary physician.
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Comparison of Teriparatide with Risedronate on Lumbar Spine Bone Mineral Density in Men and Postmenopausal Women with Low Bone Mass and a Recent Pertrochanteric Hip FracturePostmenopausal Women and Men with Low Bone Mass and a Recent Pertrochanteric FractureMedDRA version: 17.1Level: LLTClassification code 10031288Term: Osteoporosis with fractureSystem Organ Class: 100000004859EUCTR2008-002693-35-SEEli Lilly and Company Ltd285
