Japan Mako Knee Registry

Japan Mako Knee Registry - Japan Mako Knee Registry

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000043551

Enrollment

500

Registered

2021-03-08

Start date

2021-02-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

knee osteoarthritis, other

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Patient is a candidate for knee arthroplasty with Mako, or patient underwent knee arthroplasty with Mako. 2) Patient has signed an Informed Patient Consent Form*. 3) Patient expects to be evaluable for 2-years observation period postoperatively*. *Not applicable for patients included with opt-out.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Effectiveness Revision rate due to poor implant placement up to 2 years postoperatively	—

Secondary

Measure	Time frame
Effectiveness -accuracy of Implant placement - Improvement of postoperative knee function (patient-based outcomes such as KSS, JOA score, FJS, etc.) - reduction of early postoperative pain (VAS score, painkillers usage) Safety incidence of intraoperative complications	—

Countries

Japan

Contacts

Public ContactKenta Suzuki

Stryker Japan K.K. Clinical Affairs

NSKclinicaltrial@stryker.com03-6894-0000

Outcome results