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Japan Mako THA study

Japan Mako THA study - Japan Mako THA study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000038805
Enrollment
400
Registered
2019-12-06
Start date
2019-12-05
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

Hip osteoarthritis

Interventions

None listed

Sponsors

Stryker Japan K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime 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

Public ContactYuko Komori

Stryker Japan K.K. Clinical Affairs

NSKclinicaltrial@stryker.com03-6894-8394

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026