Reverse Shoulder Prosthesis Study — RSP

Rotator Cuff Arthropathy Clinical Trial

Official title:
Encore Reverse Shoulder Prosthesis

Status Completed

Clinical Trial Summary

The objective of this clinical study is to evaluate the safety and efficacy of the Encore Reverse Shoulder Prosthesis (RSP). The clinical results of the RSP will be compared to clinical results published in literature for rotator cuff arthropathy and salvage procedures.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00764504
Study type	Interventional
Source	Encore Medical, L.P.
Contact
Status	Completed
Phase	Phase 3
Start date	October 2002
Completion date	August 2008

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT04864158` - Prosthesis Versus Active Exercise Program in Patients With Rotator Cuff Arthropathy	N/A
Recruiting	`NCT05847062` - Clinical Trial to Analyze Lateralized Models and Medializations of Inverted Arthroplasty.	N/A
Active, not recruiting	`NCT04809077` - Focus on the Humeral Component Following Reverse Shoulder Arthroplasty	N/A
Completed	`NCT04405947` - Influenze of Approach in Reversed Shoulder Prosthesis	N/A