TESS Shoulder Arthroplasty Data Collection

Zimmer Biomet

Status: Terminated

Conditions: Arthritis

Study type: Observational

Funder types: Industry

Identifiers

NCT00751673

BMETEU.CR.EU74

Details and patient eligibility

About

This observational study intends to collect efficacy and safety data on TESS shoulder system

Full description

The T.E.S.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.

Enrollment: 600 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

600 participants in 1 patient group

TESS prosthesis

Description:

Consecutive series of patients with a TESS prosthesis.