Clinical Trials Directory

Trials / Terminated

TerminatedNCT00754416

S.E.S Shoulder Arthroplasty Data Collection

A Prospective, Multicentre Study Evaluating the Clinical Performance of the S.E.S Shoulder Prosthesis

Status
Terminated
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
Zimmer Biomet · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This observational study intends to collect efficacy and safety data on S.E.S shoulder system

Detailed description

The S.E.S.® shoulder system has been developed to provide a complete solution for all the indications for Shoulder Arthroplasty, Arthritis, Rotator Cuff Arthropathy, Proximal Humeral Fracture, minimising bone resection and restoring the natural anatomy of the patient.

Conditions

Timeline

Start date
2003-03-01
Primary completion
2016-09-01
Completion
2016-09-01
First posted
2008-09-18
Last updated
2017-03-07

Locations

12 sites across 2 countries: Belgium, France

Source: ClinicalTrials.gov record NCT00754416. Inclusion in this directory is not an endorsement.