RecruitingNCT05044767
Study to Evaluate the Performance and Safety of ATF Implants and Lapé Médical Devices Implanted During Hip Arthroplasty
Observational and Prospective Multicenter Study to Evaluate the Long-term (10 Years) Performance and Safety (10 Years) of ATF Implants and Lapé Médical Devices Implanted During Total Hip Arthroplasty or Hemiarthroplasty.
Sponsor
ATF Implants
Enrollment
4,500 participants
Start Date
Jun 7, 2021
Study Type
OBSERVATIONAL
Conditions
Summary
Observational and prospective multicenter study to evaluate the long-term (10 years) performance and safety (10 years) of ATF Implants and Lapé Médical devices implanted during total hip arthroplasty or hemiarthroplasty.
Eligibility
Inclusion Criteria17
- Male or female indicated for hip replacement surgery with hip prosthesis manufactured by ATF Implants and/or Lapé médical;
- There are different indications for hip replacement surgery. The main ones are listed below:
- Dysplasia
- Primary Coxarthrosis
- Secondary Coxarthrosis
- Perthes disease
- Epiphysiolysis
- Ankylosing spondylitis
- Trochanteric bursitis
- Arthritis
- Degenerative arthritis
- Post-traumatic arthritis
- Rheumatoid arthritis
- Femoral neck fracture
- Osteonecrosis
- Revision
- Depending on the specificities of the devices (size, absence/presence of a coating, material), indications may vary. This information can be found in the instruction for use. It is the surgeon's responsibility to select the most appropriate prosthesis for a given patient according to the patient's medical records and the instruction for use in force at the time of the procedure accompanying the medical device.
Exclusion Criteria6
- There are various contraindications for hip arthroplasty. The main ones are listed below:
- An acute or chronic, local or systemic infection
- Severe muscular, neurological or vascular deficiency compromising the affected extremity
- A bone defect or insufficient bone quality that may compromise the stability of the implant
- Any concomitant disease (dysplastic coxarthrosis with extreme coxa valga, short neck and severe varus) that may affect the function of the implant
- Sensitivity to the material (allergy) Depending on the specificities of the devices (size, absence/presence of a coating, material), contraindications may vary. This information can be found in the instruction for use of the devices.
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Interventions
DEVICEtotal hip arthroplasty
hip replacement surgery
Locations(13)
View Full Details on ClinicalTrials.gov
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NCT05044767