NL-OMON54026已完成不适用
A prospective, multicenter, randomized, parallel-group controlled trial to compare conservative versus surgical treatment of foot drop in peroneal nerve entrapment. - FOOTDROP
niversitaire ziekenhuizen Leuven0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 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
- •1. Written informed consent to participate in the study must be obtained from
- •the subject or proxy / legal representative prior to initiation of any
- •study-mandated procedure
- •2. EDX-documented peroneal nerve entrapment with persisting (10 ± 4 weeks) foot
- •drop (MRC-score <= 3)
- •3. Imaging (ultrasound/MRI) performed to exclude a compressive mass
- •4. Age >= 18 years
排除标准
- •1. Subjects with posttraumatic or iatrogenic peroneal nerve injury
- •2. Subjects with peroneal neuropathy due to a compressive mass (e.g. cyst,
- •3. Peroneal nerve entrapment at other sites than the fibular head
- •4. Bilateral peroneal nerve entrapment
- •5. Patients with mental or physical problems that incapacitate them to
- •participate in a physiotherapy program
- •6. Psychiatric illness
- •7. Pregnancy
- •8. Planned (e)migration within 1 year after randomization to another country
- •9. Subjects with previous foot drop
- •10. Permanently bedridden subjects
- •11. Subjects with neurological or musculoskeletal history which could impact
- •foot drop assessment and/or gait analysis (e.g. polyneuropathy, hereditary
- •neuropathy with pressure palsies, critical illness polyneuropathy, previous
- •stroke, ankle surgery, ankle sprain, *).
研究者
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