Anterior approach to total hip arthroplasty (THA) provides superior long term outcomes when compared to posterior THA.
ID
Bron
Verkorte titel
Aandoening
Osteoarthritis, or other indication for total hip replacement surgery
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Long term PROMs (Patient Reported Outcome Measures), the Oxford Hip Score at six weeks, anterior vs posterior approach
Achtergrond van het onderzoek
Comparison of anterior versus posterior hip replacements with follow up up to one year postoperatively. Information collected is type of approach, recovery PROMs (Oxford hip score, EQ-5D-5L) pain scores, patient satisfaction. Time points are preoperative (baseline), 6 weeks postoperative, 6 months postoperative and one year.
Doel van het onderzoek
Anterior approach to total hip arthroplasty (THA) provides superior long term outcomes when compared to posterior THA.
Onderzoeksopzet
Preoperative (baseline), six weeks postoperative, six months postoperative, one year postoperative
Onderzoeksproduct en/of interventie
Patients undergoing the direct anterior or posterior approach for THA were and shall be approached, informed consent given, and enrolled. Data shall be collected on surgical technique, complications. Follow-up is by a research assistant preoperatively (baseline), and then at six weeks postoperatively, six months postoperatively and one year postoperatively.
Scores collected are the Oxford Hip Score, the EQ-5D-5L Score, patient satisfaction.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
All consecutive adult total hip arthroplasty patients at FMC (Flinders Medical Centre) and NHS (Noarlunga Health Services).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Inability to give first person consent
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiƫnten Data (IPD)
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In overige registers
Register | ID |
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NTR-new | NL9803 |
Ander register | METC FMC SALHN : The local Human Research Ethics Committee granted multi-centre approval (SALHN/329.17). |