T84.0 Z96
Conditions
Interventions
Group 1: Patients who received a metaphyseal cone during revision knee arthroplasty surgery are invited to participate in the study. X-rays are taken as part of the follow-up examination according to
Sponsors
Orthopädische Klinik der Medizinischen Hochschule im Diakovere Annastift
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - male and female patients aged 18 and over at the time of enrollment - Use of a metaphyseal cone for revision knee arthroplasty
Exclusion criteria
Exclusion criteria: - New revision in the sense of removing or replacing the Cone-fixed prosthesis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Radiological implant survival Patients are invited to a follow-up appointment as part of the study. Previously, patients had to undergo follow-up examinations (3 months, 6 months, 1 year postoperatively) according to the orthopedic routine after complex knee surgery. The short clinical-radiological follow-up periods within the first years result from the evaluation of the osteointegration of cementless implants in order to be able to determine early loosening. On the day of the follow-up, a routine x-ray check is made in two levels to check the current prosthesis position and bone integrity. | — |
Secondary
| Measure | Time frame |
|---|---|
| Description of clinical outcomes and patient satisfaction Patients are invited to a follow-up appointment as part of the study. In this follow-up examination there is also a clinical examination with determination of the range of motion, control of the peripheral blood circulation, motor skills and sensitivity and the examination of the band stability. Furthermore, the clinical outcome at the time of the follow-up examination is analyzed on the basis of established scores (WOMAC, knee society score, VAS regarding pain, UCLA score for sports activity). | — |
Countries
Germany
Contacts
Public ContactYvonne Noll
Orthopädische Klinik der Medizinischen Hochschule Hannover im Diakovere Annastift, Leitung Klinisches Studienmanagement
Outcome results
None listed