DRKS00021739已完成未知
Multi-centre, randomised, controlled, single-blinded clinical trial to prove the effectiveness of an active motion device (CAMOped) for home-use in the treatment of ruptures of the anterior cruciate ligament in addition to standardised physiotherapy rehabilitation. - CAn MObility Postoperatively Enhance Direct rehabilitation (CAMOPED)
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- OPED GmbH
- 入组人数
- 105
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
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •planned surgical treatment of a rupture of the anterior cruciate ligament
排除标准
- •- Poor compliance or mental disorders
- •- Non-consentability
- •- Participation in another clinical study -Acute or chronic injury / restriction of the contralateral side
- •- Luxation of the knee joint
- •- Injury to the posterior cruciate ligament (from Schenck II)
- •- Sideband injury (MSB and LSB) > Grade I
- •- Cartilage damage in need of intervention that leads to a modification of the post-treatment scheme
- •- Operation of the lower extremity in the last 6 months
- •- Recurrent knee surgery, ACL revision surgery
- •- Neurological diseases
- •- Basic muscular diseases
- •- Injuries to the ankle or hip joint
- •- Clinical Gonarthrosis
- •- Chronic anteroposterior instability, chronic meniscopathy, cartilage defects or other diseases of the knee joint
- •- Limitation of movement through surgical procedures
- •- Postoperative infection (exclusion in ongoing study)
- •- Condition after deep vein thrombosis of the legs
- •- Clinically relevant pAVK
- •- Passive ROM < 70°
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