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Determining rotational error in CAS revision total knee arthroplasty: a comparison with a conventional arthroplasty

Determining rotational error in CAS revision total knee arthroplasty: a comparison with a conventional arthroplasty - Determining rotational error in CAS rTKA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37410
Enrollment
44
Registered
2013-01-08
Start date
2013-12-19
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

revision of a total new knee Revision total knee arthroplasty

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with a minimum age of 18 years who will be admitted for rTKA between September 2012 and September 2015 will be included in the intervention group. ;Patients with a minimum age of 18 years who were admitted for rTKA between January 2002 and April 2012 will be included in the control group. Patients will only be included in the historical control group if a type of prosthesis was implanted which is still used today.;Only total revisions, re-implantations and partial revisions of either the tibial or femoral part are included. For partial revisions, only measurements of the part of the prosthesis which is or will be revised will be used in this study.

Exclusion criteria

Exclusion criteria: Patients who underwent or will undergo a partial revision without total revision of the tibial or femoral part and patients who received or will receive a tumor prosthesis will be excluded. Also patients with a limited knowledge of the Dutch language or who are mentally incapable for participation will be excluded.

Design outcomes

Primary

MeasureTime frame
Main study parameter is the percentage of outliers for rotational prosthesis alignment.

Secondary

MeasureTime frame
NA.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)