NL-OMON44464招募中不适用
A prospective trial on the clinical efficacy of the Ankle Spacer for the surgical treatment of large, multiple, cystic and secondary or tertiary osteochondral defects of the talus. - AS: Ankle Spacer
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 25
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
- 18 至 99(—)
入选标准
- •- age ranging from 18 to 80 years;
- •- talar osteochondral defect (multiple degenerative talar cysts present, and/or prior failed surgical treatment and/or multiple defects and/or large (>15mm))
- •- willing to receive surgical implantation of the Ankle Spacer
- •- has been informed of the nature of the study and provided written consent
- •- The subject and treating physician agree that the subject will return for all required post-procedure follow-up visits
- •- failed previous conservative treatment
- •- complaints for at least 6 months
排除标准
- •- severe ankle malalignement.(> 5° varus/valgus).
- •- fracture < 6 months
- •- tendinitis
- •- diabetes mellitus / reumathoid arthritis
- •- advanced osteoporosis
- •- grade two or higher (Kellgren-Lawrence-Score) ankle joint degeneration on the tibia side.
- •- any ankle deformation that does not allow proper rasping of the cartilage and/or proper seating of the desired sized implant, as described in the surgical technique.
- •- blood supply limitations and previous infections, which may retard healing.
- •- foreign-body sensitivity. Where material sensitivity is suspected, appropriate tests should be made and sensitivity ruled out prior to implantation.
- •- active infection or blood supply limitations.
- •- conditions that tend to limit the patient's ability or willingness to restrict activities or follow directions during the healing period, including severe neuro-arthropathy.
- •- pathological conditions, such as insufficient quantity or quality of bone (e.g., cystic changes or severe osteopenia), which may compromise implant fixation.
- •- currently participating in an investigational drug or another device study that clinically interferes with the current study endpoints.
- •- Inability to be brought back to the surgery site for long term follow-up evaluations or the subject is unwilling to fill out the appropriate evaluation forms
- •- adiposity grade I (BMI > 30 kg/m2)
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