Project period | Pre-hospitalization/Screening | Hospitalisation | Follow-up | ||||
---|---|---|---|---|---|---|---|
Assessment | 1 | 2 | 3 | 4 | 5 | 6 | 7 |
Time | Day 0 | Length of stay | 6 weeks ± 2 weeks | 12 weeks ± 3 weeks | 6 months  ± 4 weeks | 12 months ± 4 weeks | 24 months ± 4 weeks |
Diagnostics (X-Ray, MRI as indicated) | x | Â | Â | Â | Â | Â | Â |
Informed Consent (Surgery and study) | x | Â | Â | Â | Â | Â | Â |
In-/Exclusion Criteria | x | Â | Â | Â | Â | Â | Â |
Pre-op. Physical examination | x | x (Day 0) | Â | Â | Â | Â | Â |
Data to be provided by the treating clinician | Â | Â | Â | Â | Â | Â | Â |
Intervention (CHOP Code) | Â | x (Day X1) | Â | Â | Â | Â | Â |
Complications | Â | x (Day 0-X2) | x | x | x | x | x |
Physical examination | x | x | x | x | x | x | x |
Data to be extracted from routine records | Â | Â | Â | Â | Â | Â | Â |
Demographics | Â | x (Day 0) | Â | Â | Â | Â | Â |
Medical history and medication | Â | x (Day 0) | Â | Â | Â | Â | Â |
Radiographic parameters | x | Â | Â | Â | Â | Â | Â |
Length of stay | Â | x (Day 0) | Â | Â | Â | Â | Â |
Complications | Â | x (Day X2) | Â | Â | Â | Â | Â |
Data to be collected by the study nurse in cooperation with the patient | Â | Â | Â | Â | Â | Â | Â |
Kujala, Tegner, Lysholm score, Banff-score | Â | x (Day 0) | x | x | x | x | x |
Patient satisfaction | Â | x (Day X2) | x | x | x | x | x |
End of rehabilitation/end of physiotherapy | Â | Â | x | x | x | x | x |
Data to be collected at the Functional Biomechanics Laboratory in cooperation with the patient | Â | Â | Â | Â | Â | Â | Â |
Isokinetic muscle strength | x | Â | Â | Â | Â | x | Â |
Gait analysis | x | Â | Â | Â | Â | x | Â |