EBRA Study AMISTEM-C FR

Status Active, not recruiting

Clinical Trial Summary

Primary objective: Evaluate femoral stem migration Secondary objective: Evaluate the performance of AMIStem H Proximal Coating at 10 years after surgery; assessment of functional recovery; radiological evaluation; reporting of complications Scores collected: HHS, OHS, PMA, UCLA

Clinical Trial Description

The main objective of the study was to evaluate the migration and performance of the AMIStem® C femoral stem at 10 years follow-up. The primary endpoint is the measurement of femoral component migration by EBRA-FCA (The Ein Bild Roentgen Analyse-femoral component analysis, Innsbruck, Austria) The secondary objectives of the study are: Evaluate the performance of the AMIStem® C stem Evaluate the function of the operated hip To evaluate the quality of life To evaluate the safety of the AMIStem® C femoral stem Evaluate the postoperative stability and fixation of the hip prosthesis ;

Study Design

Related Conditions & MeSH terms

Total Hip Arthroplasty

Clinical Trial Details

NCT number	NCT05848024
Study type	Observational
Source	Medacta International SA
Contact
Status	Active, not recruiting
Phase
Start date	February 8, 2017
Completion date	February 2029

View Details

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