Retention of the posterior cruciate ligament versus the posterior stabilized design in total knee arthroplasty: a prospective randomized controlled clinical trial

Retention of the posterior cruciate ligament versus the posterior stabilized design in total knee arthroplasty: a prospective randomized controlled clinical trial - Retention versus sacrifice of the PCL in total knee arthroplasty.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON30597

Enrollment

120

Registered

2007-08-22

Start date

2008-01-28

Completion date

Unknown

Last updated

2024-08-12

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

Conditions

osteoarthrosis of the knee joint

Interventions

60 patients receiving the posterior stabilized total knee arthroplasty, 60 patients receiving the posterior cruciate ligament retaining total knee arthroplasty

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: primary symptomatic osteoarthrosis of the knee non fixed varus and valgus deformity of less than 10 degrees age between 55 and 85 years BMI less than 35 kg/m2 ASA I and II

Exclusion criteria

Exclusion criteria: secondary osteoarthrosis of the knee (active) arthritis (eg rheumatic disease) flexion less than 90 degrees flexion contracture over 10 degrees peripheral neuropathy history of CVA

Design outcomes

Primary

Measure	Time frame
Patients perceived outcome after TKA as determined with the WOMAC questionnaire.	—

Secondary

Measure	Time frame
Range of motion Knee Society Clinical Rating System as physician-based outcome score after TKA. Quality of Life as determined with the Short Form 36 (SF-36) Gait parameters Femoral roll back	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)