M23.99 M94
Conditions
Interventions
Group 1: The "training group" will perform three sessions a week of strength and sensorimotor training during up to six weeks between the arthroscopic cartilage biopsie and the open knee surgery for
Sponsors
Univertitätsklinikum Freiburg
Department Orthopädie und Traumatologie
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Patients with isolated symptomatic cartilage defect of the knee joint, planned autologues chondrocyte implantation and signed informed consent
Exclusion criteria
Exclusion criteria: Instability of the knee joint, serious previous surgery, pre-existing neuromuscular conditions, compliance issues (e.g. patient lives too far away from rehabilitation center)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functionality of the knee joint 12 months post-surgery (based on the validated "IKDC - international knee documentation" - 2000 Score (Brittberg et al, JBJS 2003, Niemeyer et al. Arthroscopy, 2010)) | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain on a visual analoge scale Subjective clinical outcome (Lysholm score and KOOS score) Functionality of the knee in activities of daily living (Chair Rise Test and Stair Climbing Test) Isokinetic muscle strength of knee flexors and knee extensors (Contrex Multijoint System) and measurement of postural control (Posturomed) at the end of the training phase (Pre-OP) as well as six and twelve months post-operatively | — |
Countries
Germany
Contacts
Public ContactAnja HIrschmüller
Univertitätsklinikum Freiburg Department Orthopädie und Traumatologie
Outcome results
None listed