Arthroplasty, Replacement, Hip Clinical Trial
Official title:
Omnifit Hydroxylapatite (HA) Hip Outcomes Study
The purpose of this study was to obtain up to 25 year post-operative data on the Omnifit Hydroxylapatite (HA) Hip System in support of the hypothesis that it is a satisfactory system for reducing implant loosening, permitting tissue bonding onto the hydroxylapatite surfaces of the implant and providing a safe, efficient, and well-functioning hip in a wide spectrum of clinical circumstances.
n/a
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
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Active, not recruiting |
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Recruiting |
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N/A | |
Completed |
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Completed |
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Phase 2 | |
Completed |
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Not yet recruiting |
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N/A | |
Recruiting |
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Low Concentration Local Anesthesia Fascia Iliaca Block for Total Hip Arthroplasty
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N/A | |
Recruiting |
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Recruiting |
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Phase 4 | |
Completed |
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Effects of Surgery Start Time on Postoperative Interleukin-6, Interleukin-8, and Cortisol
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N/A | |
Recruiting |
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N/A | |
Completed |
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Terminated |
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Completed |
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N/A | |
Completed |
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Phase 3 | |
Completed |
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Completed |
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Recruiting |
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N/A | |
Completed |
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N/A |