Encore Revelation Hip Stem

Completed

Conditions studied: Osteoarthritis, Hip, Complications; Arthroplasty

In brief

The purpose of this study is to obtain long-term (10+ yrs) clinical and patient outcomes data on patients who received the Revelation Hip Stem prior to 2002.

Key facts

Study ID

NCT01514318

Run by

Encore Medical, L.P.

People needed

8

Starts

2012-02-01

Expected to finish

2012-07-01

Last updated by the study team

2012-11-30

Who can join

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

You may qualify if…

• Subjects must have received the Revelation™ Hip Stem as part of a total hip arthroplasty prior to 2002.
• Surgery must have been a primary total hip replacement
• Subject must have received only one primary hip replacement per hospitalization
• Subject must have had a diagnosis of inflammatory tissue disorder, osteoarthritis, post-traumatic arthritis/secondary arthritis or avascular necrosis
• Subject must be willing and able to sign the informed consent document

You may not qualify if…

• Subject must not have had any previous hip implants (hemi or total joint)
• Subject has a mental condition that may interfere with the ability to give an informed consent (i.e., severe mental retardation such that the subject cannot understand the informed consent process, global dementia, prior strokes that interfere with the subject's cognitive abilities, senile dementia, and Alzheimer's Disease)
• Subject is a prisoner
• Subject is pregnant

Where it is running

• Westlake Orthopaedics Spine & Sports — Austin, Texas, United States

Full record on ClinicalTrials.gov

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