DRKS00000144已完成不适用
A prospective, non-blinded, randomised study to examine the influence of surgical approach on function, electrical muscle activity and periprosthetic bone mineral density after implantation of a hip endoprosthesis - Periprosthetische Knochendichte nach TEP
niversitätsmedizin BerlinCharité Campus MitteCentrum für Muskuloskeletale ChirurgieOrthopädische Klinik0 个研究点目标入组 100 人开始时间: 2009年6月23日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
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
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- one 至 80 Years（—）
- 性别
- All
入选标准
- •1. Males or females with coxarthrosis for which cement-free implantation is indicated.
- •2. Written informed consent of patient.
排除标准
- •1. Pregnancy.
- •2. Patients in whom the indication for implantation of the hip endoprosthesis is due to a high level of dysplasia or a congenital luxation.
- •3. Patients in whom exists the indication for implantation of a cemented hip endoprosthesis.
- •4. Patients who have already undergone an operation in any other area of the hips or the rest of pelvis or are older than 80 years.
- •5. Patients in whom there is advanced arthrosis or arthrodesis in another joint of the lower extremity.
- •6. Patients with functionally poor endoprosthesis of the lower extremity.
- •7. Patients with severe spinal degeneration and / or deformation.
- •8. Patients with overt osteoporosis or patients for which a permanent medication (eg corticosteroids, anticoagulants) resulting in changes in bone density can be expected.
- •9. Patients with tumors in the pelvis or the femur.
- •10. Patients who have already received local radiation treatment for tumors in the area of the pelvis and the femur.
- •11. Patients who are ill are in a dispute.
- •12. Patients who have limited legal capacity or incapacity.
研究者
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