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临床试验/JPRN-UMIN000010625
JPRN-UMIN000010625已完成未知

The survey study of Dual-Mobility-THA for femoral neck fracture, on the indication and the efficacy/safety - DM THA Study

Stryker Japan K.K.0 个研究点目标入组 50 人开始时间: 2013年7月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients have bacterial infectious disease or have risk highly of bacterial infection. 2) Patients have treatment history of acetabulum/ femur. 3) Patients, who are morbidly obese, defined as having a Body Mass Index (BMI) > 40. 4) Patients who is pregnant female or maybe so. 5) Patients who have a neuromuscular or neurosensory deficiency, which limits ability to evaluate the safety and efficacy of the device. 6) Patients with diagnosed systemic disease (i.e. Paget's disease, renal osteodystrophy), which limits ability to evaluate the safety and efficacy of the device. 7) Patients who are immunologically suppressed or receiving chronic steroids, which limits ability to evaluate the safety and efficacy of the device. 8) Patients who are judged ineligible with reasonable reason by primary doctor.

研究者

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