Clinical, functional and psychosocial outcome of shoulder prothesis

• Conditions: M19.21; M75.1; Rotator cuff syndrome

• Registration Number: DRKS00010934
• Lead Sponsor: Deutsche Gesellschaft für Ultraschall in der Medizin (DEGUM) e.V.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-10-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 63

Inclusion Criteria

Patients with the indication for a reverse shoulder arthroplasty; healthy subjects

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: observational
• 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; 6 and 24 months postoperatively

Secondary Outcome Measures

Name	Time	Method
Development of the perfusion in deltoid muscle tissue, assessed with contrast-enhanced ultrasound; 6 and 24 months postoperatively