THis study is aimed to provide a clinical and radiographic evaluation of 49 suitable subjects who underwent a total hip arthroplasty with DELTA Revision acetabular cup.
This is an observational study designed to reflect real life clinical practice as closely as possible. Thus, clinicians are free to choose the method to implant and total hip arthroplasty in accordance with the current local Delta Revision acetabular cup Indication for Use and current clinical practice.
Study Type
OBSERVATIONAL
Enrollment
49
Total hip arthroplasty
Samodzielny Publiczny Szpital Kliniczny im. Prof. Adama Grucy CMKP
Otwock, Poland
RECRUITINGHarris Hip Score (HHS)
Overall score from 0 to 100, with 100 being the best outcome
Time frame: From preoperative to 2 years after surgery
ROM measurement
Functional changes in ROM measurements from pre-operative (baseline), discharge, 2 months, 6 months, 1 year and 2 years
Time frame: From preoperative to 2 years after surgery
Oxforn Hip Score (OHS)
Overall score from 0 to 48, with 48 being the best outcome
Time frame: From preoperative to 2 years after surgery
Survival rate
Survival rate expressed with Kaplan-Meier estimator at 2 years after surgery
Time frame: 2 years
Radiographic implant evaluation and stability assessment of the DELTA Revision acetabular cup
The treated hip is analyzed postoperatively based on anteroposterior and lateral x-rays view of the knee to check for radiographic stability and radiographically detectable complications
Time frame: From preoperative to 2 years after surgery
Incidence, type and severity of all the Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Device Effects (ADEs), and Serious Adverse Device Effects (SADEs) occurred at each follow-up
Time frame: From preoperative to 2 years after surgery
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