2Y-FU-PSI-UKA

2 Years Follow-up of patient-specific matched instruments for unicompartmental knee arthroplasty A prospective cohort study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON23303

Enrollment

120

Registered

2017-02-09

Start date

2017-03-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

This cohort study will evaluate patients who have been operated for knee arthroplasty (UKA) according to the Signature alignment method.

Interventions

A relatively new technique for the perioperative alignment of prosthesis components inunicompartmental knee arthroplasty (UKA) is the use of patient-specific guiding (PSG). The guides used in this tec

Eligibility

Inclusion criteria

Inclusion criteria: • Patients who received UKA using PSG • Patients who complete the preoperative and follow-up at 3 months, 1 and 2-years • Patients of whom digital radiographs are available

Exclusion criteria

Exclusion criteria: • Patients who failed to complete follow-up • Patients of whom no digital radiographs are available • Patients of whom digital radiographs are of poor quality

Design outcomes

Primary

Measure	Time frame
Implant alignment and survival	—

Contacts

Public ContactM.G.M. Schotanus

Department of Orthopedic Surgery, Zuyderland Medisch Centrum dr H vd Hoffplein 1

m.schotanus@zuyderland.nl+31 (0)88 4597823

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)