S.E.S Shoulder Arthroplasty Data Collection

Zimmer Biomet100 enrolled

Overview

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

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.

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Arthritis

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * A pre-operative level of pain and function the same as for conventional joint replacement * A likelihood of obtaining relief of pain and improved function * Full skeletal maturity * Ability to follow instructions * Good general health for age * Willing to return for follow-up evaluations Exclusion Criteria: * Glenohumeral joint infection, osteomyelitis * Neuro-muscular complications * Inability to co-operate with and complete the study

Locations (12)

De Dreef Van Zonnebos 13

Schilde, Belgium

Clinique Générale

Annecy, France

Clinique St Joseph

Chambéry, France

Centre Hospitalier Général

Dax, France

Outcomes

Primary Outcomes

Constance and oxford Scores

Time frame: 6m, 1yr, 2yr, 3yr, 4yr and 5 yr

Secondary Outcomes

Complication

Time frame: Any time

Patient Satisfaction

Time frame: 6m,1yr,2yr,3yr,4yr and 5yr

Data from ClinicalTrials.gov

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