Inducible Displacement in Total Knee Prostheses

MC is the sponsor of the study0 个研究点目标入组 30 人开始时间: 待定最近更新: 2024年2月28日

适应症

试验速览

暂无简介。

•Patients will be included if
•they underwent TKR for primary as well as secondary gonarthrosis as long as the indication for surgery is
•clearly specified
•a minimal set of patient characteristics (age, gender, BMI, co-morbidity) and disease characteristics
•(radiological severity, knee function and alignment, status of other knee or hip joints, previous surgeries of the
•affected knee) is available.
•they are at least `up to date' in terms of follow-up of their respective study (i.e. the most recent examination was
•less than a year ago and patients have apost-operative examination)
•they participated for at least three years in their respective study and have a usable MTPM-value (i.e. >_ 3 bonemarkers
•can be consistently matched with the reference-examination with a CN < 120 over the most recent iwo
•years of fol low-u p
•their standard RSA data meets the criteria as mentioned in the ISO-standard
•they are willing to participate and able to perform the 4 pre-set tasks for the inducible displacement

•Patients will be excluded from participation if they do not meet the inclusion criteria, or if they already underwent
•revision surgery of their TKR since the start of the study they were enrolled in.

发起方

MC is the sponsor of the study