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Clinical Trial Summary

Two-year (2 year) information regarding the performance of the commercially available Actis™ Total Hip System in order to obtain and evaluate the clinical outcomes on a series of cementless primary total hip arthroplasty (THA) and hemi-hip arthroplasty procedures using clinical, radiographic and device and procedure related adverse event assessments.


Clinical Trial Description

A minimum of 10 study sites. A prospective, uncontrolled, non-randomized, multicenter study. A total of 255 Subjects to include a minimum of 225 Primary THA Subjects and a Sub-group with a minimum of 30 hemi-hip arthroplasty Subjects will be prospectively enrolled into the study. All Subjects will be seen for a preoperative clinic visit at the time of consent, and evaluated at the time of surgery, 6 weeks (28-70 days), 3 months (71-132 days), minimum 1 year (304-668 days), and minimum 2 years (669-1,763 days) postoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02783274
Study type Interventional
Source DePuy Orthopaedics
Contact Kirstin Cosgrove, BS
Phone 714-420-4589
Email KCosgro1@its.jnj.com
Status Recruiting
Phase N/A
Start date July 1, 2016
Completion date July 1, 2024

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