FUJI Study (Functional evaluation Using JOURNEY Implant)

FUJI Study (Functional evaluation Using JOURNEY Implant) - FUJI Study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000015347

Enrollment

672

Registered

2016-10-16

Start date

2014-10-01

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

Total Knee Arthroplasty

Interventions

JOURNEY II BCS Conventional total knee system

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Subject requires primary total knee arthroplasty 2) Subject has knee osteoarthritis

Exclusion criteria

Exclusion criteria: 1) Subject has dementia 2) Subject has rheumatoid arthritis of knee 3) Subject after high tibial osteotomy 4) Subject after fracture of lower limb (Subject after knee arthroscopy and subject has bilateral knee osteoarthritis)

Design outcomes

Primary

Measure	Time frame
2011 New Knee Society Score Satisfaction	—

Secondary

Measure	Time frame
2011 New Knee Society Score Functional Charnley Functional Classification, Alignment, Stability, ROM, Expactation, Activity, UCLA Activity Score, Range of Motion Pain Evaluation etc.	—

Countries

Japan

Contacts

Public ContactShigeshi Mori

Kinki University Faculty of Medicine, Department of Orthopaedics

smori@med.kindai.ac.jp072-366-0221

Outcome results

None listed

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