A Clinical Investigation of the Comprehensive®, BioModular®, and Bi-Angular® Shoulder Systems

Zimmer Biomet

Status: Withdrawn

Conditions: Humeral Fractures; Osteoarthritis; Avascular Necrosis; Rheumatoid Arthritis

Study type: Observational

Funder types: Industry

Identifiers

NCT00699270

Biomet 12380-76

Details and patient eligibility

About

The purpose of this prospective clinical data collection is to document the performance and clinical outcomes of Biomet Humeral Stems

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
• Rheumatoid Arthritis
• Correction of functional deformity

Exclusion criteria

Absolute contraindications:

• Infection, Sepsis, and Osteomyelitis

Relative contraindications:

• Uncooperative patient or patient with neurologic disorders who is incapable or unwilling to follow directions
• Osteoporosis
• Metabolic disorders which may impair bone function
• Osteomalacia
• Distant foci of infections which may spread to the implant site
• Rapid joint destruction, marked bone loss or bone resorption apparent on roentgenogram

Trial design

0 participants in 1 patient group

Biomet Humeral Stems

Description:

Biomet Humeral Stems: Comprehensive®, BioModular®, and Bi-Angular® Shoulder Systems