Biomet Humeral Stem Data Collection

Stopped early · Not applicable

Conditions studied: Humeral Stem Replacement

In brief

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

Key facts

Study ID

NCT00553527

Run by

Vanderbilt University

People needed

2

Starts

2007-07-01

Expected to finish

2009-07-01

Last updated by the study team

2009-08-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
• Rheumatoid Arthritis
• Correction of functional deformity
• Patient selection factors to be considered:
• Need to obtain pain relief and improve function
• Ability and willingness of the patient to follow instructions, including control of weight and activity levels
• A good nutritional state of the patient
• The patient must have reached full skeletal maturity

You may not qualify if…

• Patients who have infection, sepsis, and osteomyelitis
• Patients who are uncooperative or have neurologic disorders who is capable or unwilling to follow directions
• Patients who have osteoporosis
• Patients who have metabolic disorders which may impair bone function
• Patients with osteomalacia
• Patients with distant foci of infections which may spread to the implant site
• Patients with rapid joint destruction, marked bone loss, or bone resorption apparent on roentgenogram
• Patients who are pregnant
• Patients who are under 18 years of age

Where it is running

• Vanderbilt Hand Center — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

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