Observational Study to Evaluate Long-Term Outcome in Hip Hemiarthroplasty

Who can take part

• Both genders
• Adult subjects
• Subjects clinically suitable for a hip hemiarthroplasty surgery with Corin hip devices based on physical examination, medical history and diagnosis such as: non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis in which the acetabulum does not require replacement, treatment of non-union, femoral neck and trochanteric fractures of the proximal femur, revision of failed partial hip replacements in which the acetabulum does not require replacement
• The subject is willing to comply with the required follow-up visits as per protocol
• The subject, or a designated trusted person in case the subject is unable to do, has signed a Patient Informed Consent Form (PICF), specific to this study, and approved by the local EC

Who cannot take part

• Subjects with active infection or sepsis or osteomyelitis
• Subject with metabolic disorders which may impair bone formation or bone quality
• Subjects in the opinion of the Investigator/ investigative team who will be unable to comply with study procedures (Examples: recent psychotic or mania disorders, alcohol, drug or substance abusers) and/or those unable for any medical or other reason to comply with study procedures/visits
• Subjects with unsuitable or insufficient bone support preventing proper fixation of the prosthesis
• Subject with marked bone loss or bone absorption
• Subjects under guardianship
• Subjects under jusicial protection