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Scorpio PS vs Scorpio NRG PS total knee arthroplasty. Comparative investigation of function.

Scorpio PS vs Scorpio NRG PS total knee arthroplasty. Comparative investigation of function. - Scorpio PS vs Scorpio NRG PS

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34832
Enrollment
88
Registered
2010-07-19
Start date
2010-09-30
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

knee arthrosis knee arthoplasty

Interventions

All patients will have a total knee replacement operation during which the study knee or the control knee prosthesis will be implanted

Sponsors

Stryker SA
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: age between 18 and 80 years male and non-pregnant female patients requiring a primary TKA

Exclusion criteria

Exclusion criteria: patients with BMI higher than 35 patients with active infection patients with malignancy patients requiring revision surgery of a previous implanted total knee system

Design outcomes

Primary

MeasureTime frame
As primary study parameter the maximal flexion will be compared between the two prostheses.

Secondary

MeasureTime frame
As secondary study parameters the complications will be registered and a comparison will be done of the chair raise and stair climb test with the corresponding pain score, and the operation time

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)