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Determining realistic prognosis of outcome of total knee arthroplasty

Determining realistic prognosis of outcome of total knee arthroplasty - Determining realistic prognosis of outcome of total knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON34734
Enrollment
180
Registered
2011-01-04
Start date
2011-01-10
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

Osteoarthritis Rheumatoid arthritis

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patient underwent total knee arthroplasty (type Total Condylar) between 1-1-1979 and 31-12-1990 at AZL/LUMC. Or patient underwent revision total knee arthroplasty between 1-1-1993 and 31-12-2009 at AZL/LUMC. Patient is capable of giving informed consent and expressing a willingness to comply with this study. Patient is able and expressing willingness of filling in questionnaires regarding their operated knee(s) and daily function

Exclusion criteria

Exclusion criteria: Patient is unable or unwilling to sign the Informed Consent specific to this study. Patient is unable or unwilling of filling in the questionnaires regarding their operated knee(s) and daily funcion.

Design outcomes

Primary

MeasureTime frame
For determining long term results of primary total knee arthroplasty, we use the following encpoint: Failure of the prosthesis, which is defined as: - removal of the prosthesis - recommended removal of the prosthesis (radiographic loosening) - clinical failure For determining the effect of preoperative parameters on clinical outcome, we use regression analysis. Following outcome measures will be used: - KSS score - patient satisfaction - quality of life - daily functioning - survival of the prosthesis

Secondary

MeasureTime frame
none

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)