Hip osteoarthritis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. The patient who will receive/received THA with Mako system. 2. The patient has signed the IRB approved, study specific informed patient consent form. (Not applicable if the site allows to enroll subject retrospectively or the patient has already received THA with Mako system.) 3. The patient who is willing to participate the study during the follow-up period. (Not applicable if the site allows to enroll subject retrospectively or the patient has already received THA with Mako system.)
Exclusion criteria
Exclusion criteria: NA
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. The discrepancy between pre-operative plan and post-operative implant position indicated in Mako system 2. The discrepancy between implant position indicated in Mako system and post-operative CT evaluation. | — |
Countries
Japan
Contacts
Stryker Japan K.K. Clinical Affairs