Multicentric, Prospective, Comparative Trial to Assess the Efficacy and Safety of an Anatomic Total Shoulder System.
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of this study is to demonstrate safety and efficacy of the Mirror Medacta Shoulder System in total shoulder arthroplasty.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Age ≥ 18 yr
• Clinical indication for anatomic primary total shoulder replacement due to osteoarthritis and/or posttraumatic arthritis
• Willingness and ability to comply with study protocol
Locations
Other Locations
Switzerland
Lindenhofgruppe AG - Orthopädie Sonnenhof
RECRUITING
Bern
Klinik für Orthopädische Chirurgie und Traumatologie des Bewegungsapparates, Kantonsspital St.Gallen
RECRUITING
Sankt Gallen
Contact Information
Primary
Marco Viganò, PhD
m.vigano@medacta.ch
+41 091 6966060
Time Frame
Start Date: 2022-01-05
Estimated Completion Date: 2027-12-30
Participants
Target number of participants: 100
Treatments
Experimental: Mirror group
Mirror Medacta Shoulder System
Active_comparator: Historical Control group
Total shoulder arthroplasty system
Related Therapeutic Areas
Sponsors
Leads: Medacta International SA