EUCTR2009-015058-38-GB进行中(未招募)1 期
Improving the outcome for patients after osteoporotic femoral fractures - Improving the outcome for patients after osteoporotic femoral fracture
niversity of Leeds0 个研究点目标入组 120 人开始时间: 2010年8月17日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 120
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
入选标准
- •- Patients with acute traumatic trochanteric or supracondylar femoral fractures and fragility fractures (i.e. sustained from standing height or less and radiological features of osteoporosis). - Patients who are aged 55 or older.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 0
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •- Patients with open fractures, pathological fractures, ‘floating knee’, associated patellar fractures or simultaneous bilateral fractures - Patients with a known metabolic bone disease, rheumatoid arthritis or chronic renal failure - Patients with dementia - Patients with bone metastases or other malignant bone disease - Patients taking steroids, strontium, biphosphonates or PTH -Patients with oesophageal abnormalities, swallowing problems, hypocalcaemia, hypercalcemia. - Women of child-bearing age (<55years), pregnant or breast feeding.
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