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clinical results according to the implant type for total knee arthroplasty (KR type vs. PS type)

Comparison of outcomes in patients with total knee arthroplasty using KR (Kinematic Retaining) type or PS (PCL Sacrificing) type prosthesis: randomized controlled study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CRIS
Registry ID
KCT0005953
Enrollment
90
Registered
2021-03-04
Start date
2021-02-26
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

None listed

Interventions

Medical Device : Patients who need total knee arthroplasty are assigned to KR group and PS group by performing randomization allocation before surgery. For the assigned group, the surgery is performed

Sponsors

Chonnam National University Hospital Hwasun Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Total knee arthroplasty is scheduled for both knee degenerative arthritis, traumatic arthritis, non-inflammatory degenerative knee arthritis, including avascular necrosis, and rheumatoid arthritis. And subjects who have been fully informed of the preoperative study and have expressed consent to participate

Exclusion criteria

Exclusion criteria: -Patients with a history of infectious arthritis in the knee joint scheduled for surgery -Subjects with decreased range of motion in the knee joint (flexion contraction more than 30 degrees, subsequent flexion less than 90 degrees) -Subjects with very severe valgus and varus deformities (Hip-Knee-Ankle angle ± 20 degrees or more) -In case of severe joint destruction and deformation, and it is expected to perform artificial joints using bone grafts, blocks, or long stems. -Subjects who have severe deformations in the femur, tibia, and patella, including around the knee joint, and are considered to affect the result analysis -If it is judged that it is inappropriate to be included in the study by the other responsible researcher

Design outcomes

Primary

MeasureTime frame
Physical examination (knee joint range of motion);Survey (Pain, Stiffness, Functional outcome, Patient Satisfaction, Expectation)

Secondary

MeasureTime frame
plain radiograph

Countries

Korea, Republic of

Contacts

Public ContactYoung Min Lee

Chonnam National University Hospital Hwasun Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026