Clinical, functional and psychosocial outcome of reverse shoulder arthroplasty - a prospective randomized comparison of two types of prostheses after traumatic fracture of the proximal humerus
Not Applicable
- Conditions
- S42.21M19.91
- Registration Number
- DRKS00011581
- Lead Sponsor
- Zentrum für Orthopädie, Unfallchirurgie und Paraplegiologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Patients with multifragmentary fracutres of the proximal humerus and indication of RSA. Patients with rotator cuff arthropathy and indication of planned RSA.
Exclusion Criteria
- known intolerance for SonoVue
- severe heart failure (NYHA III/IV)
- myocardial infarction within the last 14 days
- severe respiratory diseases
- pregnancy and breastfeeding
- age under 18 years
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Shoulder function: Constant-Murley-, ASES-, DASH-Score, Simple Shoulder Test;<br>Psychosocial outcome: SF-12;<br>Pain: visual analogue scale; <br>radiological outcome: x-ray;<br>6 and 24 months postoperatively<br>
- Secondary Outcome Measures
Name Time Method Development of the perfusion in deltoid muscle tissue, assessed with contrast-enhanced ultrasound; 6 and 24 months postoperatively