hip osteoarthritis, other
Conditions
Interventions
None listed
Sponsors
Stryker Japan K.K.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patient underwent Total hip arthroplasty with Mako system. 2) Patient has signed an Informed Patient Consent Form*. 3) Patient is willing to continue participating during the study observation period *. *Not applicable for patients included with opt-out. *Not set inclusion criteria for historical control group, who underwent THA by conventional or computer assisted surgery.
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The number of screws for cup fixation | — |
Secondary
| Measure | Time frame |
|---|---|
| -Cup fixation at 3 months after the procedure -Deviation of cup alignment between plan and post-op. -Placement rate in Lewinnek/Callanan safe zones. -Usage of bone augment | — |
Countries
Japan
Contacts
Public ContactYuko Komori
Stryker Japan K.K. Clinical Affairs
Outcome results
None listed