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临床试验/DRKS00030880
DRKS00030880招募中Unknown

Postoperative rehabilition after reverse shoulder arthroplasty withelectric muscle stimulation

OCM Klinik0 个研究点目标入组 34 人开始时间: 2023年7月4日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
34

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

  • Patient specific inclusion criteria:
  • 1. Patient of legal age (m/f/d) and capable of consent with a
  • 2. Primary osteoarthritis with rotator cuff lesion or
  • 3. Massive rotator cuff lesion or
  • 4. Cuff tear arthropathy, that was
  • 5. treated by a reverse shoulder arthroplasty.
  • Case specific inclusion criteria:
  • 1. Treatment of the given pathologies of the shoulder with a uncemented reverse shoulder arthroplasty using
  • 2. The same uncemented short stem (Aequalis Ascend Flex, Stryker).
  • 3. Start of intervention between 12 to 24 months after the surgery.

排除标准

  • 1. Unable to contact for recruitment due to missing/outdated contact information/data
  • 2. Cases with a acute fracture, avascular necrosis or revision cases
  • 3. Prior surgery on the affected shoulder or
  • 4. Postoperative complications (periprosthetic fracture, loosening, infection etc.) with or without a revision of the case
  • 5. Contraindications to a therapy using electric stimulation around the shoulder
  • 6. Secondary illnesses, that affect the connective tissue (e.g. Marfan syndrome, Ehlers-Danlos syndrome, scleroderma)
  • 7. Secondary illnesses, that affect the nervous system (e.g. parkinsons disease, multiple sclerosis, peripheral neuropathy)
  • 8. Secondary illnesses, that affect the muscle tissue (e.g. Mitochondrial myopathies, muscular dystrophies, myotonic syndromes)
  • 9. Secondary rheumatic diseases.

研究者

发起方
OCM Klinik

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