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Observational Study to Evaluate Long-Term Outcome in Hip Hemiarthroplasty

This trial has no sites in United States.

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  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

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Trial details

Who runs it
Corin
Trial code
NCT05686278
Record updated
18 March 2026
Original description
This PMCF study is designed to collect safety and efficacy data on hip hemiarthroplasty surgeries with Corin BiPolar-i shell and the Oceane+ or Meije Duo femoral stem up to 10 years.Read full original descriptionShow less

A Post-market Clinical Follow-up (PMCF) Study to Evaluate Clinical, Radiographic and Patient Reported Outcomes Following a Hip Hemiarthroplasty Surgery Using Corin Devices

This PMCF study is designed to collect safety and efficacy data on hip hemiarthroplasty surgeries with Corin BiPolar-i shell and the Oceane+ or Meije Duo femoral stem up to 10 years.

Inclusion: 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.

Exclusion: 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.

ClinicalTrials.gov NCT05686278