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Actis Total Hip System 2 Year Follow-up
Principal Investigator (?)
Study Number
F16103
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. 
Phase (?)
Phase III
Sponsor (?)
Contact

Peter DePalo Sr.

Available at the following location(s)

Lebanon

View more details from ClinicalTrials.gov.

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