Multicentre SMS Study - FR

Exclusion Criteria

• •Participation in biomedical research.
• •Minor patient.
• •Protected adult patient.
• •Vulnerable individuals as defined by Article L1121-6 of the Public Health Code.
• •Pregnant or breastfeeding women.
• •Patient unable to express their non-opposition.
• •Patient refusing the collection of their personal data.
• •Acute, systemic, or chronic infection. Skeletal immaturity.
• •Grossly deformed anatomy (at the surgeon's discretion).
• •Osteomalacia for which the fixation of an uncemented implant is contraindicated.
• •Patient suffering from active rheumatoid arthritis or osteoporosis.
• •Patient with metabolic disorders likely to impair bone formation when the fixation of an uncemented implant is contraindicated.
• •Patient suffering from muscle atrophy or neuromuscular disease.
• •Patient with an allergy to the implant material.
• •Any patient who cannot or does not wish to give their informed consent to participate in the study.
• •Patient whose prospects of regaining independent mobility would be compromised by known coexisting medical problems.
• •Any contraindication mentioned in the instructions for use of the investigational medical device.