Postoperative rehabilition after reverse shoulder arthroplasty withelectric muscle stimulatio
- Conditions
- Z96.60
- Registration Number
- DRKS00030880
- Lead Sponsor
- OCM Klinik
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 34
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.
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 Unable to contact for recruitment due to missing/outdated contact information/data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.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Contant Shoulder Score
- Secondary Outcome Measures
Name Time Method Range of Motion, Subjective Shoulder Value