Pre-operative templating by use of MRI in primary total knee replacement

Pre-operative templating by use of MRI in primary total knee replacement - Templating total knie replacement by MRI

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON32957

Enrollment

Registered

2009-10-27

Start date

2009-07-01

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

cartilage damage Knee arthrosis

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with knee osteoarthritis undergoing a total knee replacement.

Exclusion criteria

Exclusion criteria: Systemic disease (e.g. rheumatoid arthritis, lupus erythemadosus), tibia plateau fracture or high tibial osteotomy in history, anterior cruciate ligament rupture in history, inability to understand the patient information (e.g. mental retardation, language barrier), patients with a contra-indication for MRI (e.g. pacemaker).

Design outcomes

Primary

Measure	Time frame
The primary outcome measures are the overall reliability and accuracy of the pre-operative template size of the MRI template method and the conventional method by use of radiographs, compared with the actually implanted prosthesis.	—

Secondary

Measure	Time frame
Secondary outcome measures are intra- and interobserver reliability of both methods.	—

Countries

Netherlands

Outcome results