A Two Centre Study to Assess the Stability and Long-term Performance of the C-Stem™ AMT in a Total Primary Hip Replacement

Exclusion Criteria

• •i) Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this study.
• •ii) Subjects undergoing revision hip replacement
• •iii) Subjects undergoing simultaneous bilateral hip replacements.
• •iv) Subjects with a contralateral hip replacement, which was implanted less than six months previously or is not performing satisfactorily.
• •v) Women who are pregnant.
• •vi) Subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.
• •vii) Subjects who have participated in a clinical study with an investigational product in the last 12 months.
• •viii) Subjects who are currently involved in any injury litigation claims.