None listed
Conditions
Interventions
Medical Device, Procedure/Surgery : All participants enrolled in this study will undergo one total hip arthroplasty procedure using the CUVIS-joint 150 robotic system. Before surgery, computed tomogra
Sponsors
Inha University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1Adults aged 50 years or older 2Patients who require primary total hip arthroplasty for a hip disorder 3Patients who voluntarily agree to participate after receiving sufficient information about the study and provide written informed consent
Exclusion criteria
Exclusion criteria: 1Patients with an active infection at the planned surgical site or signs of systemic infection 2Patients who require revision surgery or revision arthroplasty because of a previous operation at the affected site. However, patients undergoing total hip arthroplasty after removal of internal fixation devices used for a previous fracture may be enrolled at the investigator’s discretion 3Patients considered unsuitable for robotic bone resection or implant fixation because of severe osteoporosis or bone loss 4Patients considered unable to undergo postoperative rehabilitation or follow-up because of a neuromuscular disorder or other condition 5Women who are pregnant or breastfeeding 6Patients who are unable to provide voluntary informed consent because of cognitive impairment or a similar condition
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Accuracy of Acetabular Cup Orientation, Incidence of Surgery-related Adverse Events | — |
Secondary
| Measure | Time frame |
|---|---|
| Gait and Physical Function Outcomes | — |
Countries
Korea, Republic of
Contacts
Public ContactHyunBin Kim
Inha University
Outcome results
None listed