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Recurrent patellar dislocation: personalised therapy or operative treatment? The REPPORT randomised trial protocol.
Arnold, Susanne; Haque, Aminul; Aujla, Manjit; Barrows, Raegan; Beard, David; Chandler, Craig; Chandler, Elizabeth; Ellard, David R; Eldridge, Jonathan; Ferreira, Manuela; Foster, Nadine E; Griffin, James; Mason, James; Mandalia, Vipul; Parsons, Helen; Ray, Georgina; Stewart, Kimberley; Thompson, Peter; Underwood, Martin; Whitehouse, Michael R; Zanganeh, Mandana; Metcalfe, Andrew; Smith, Toby.
Afiliação
  • Arnold S; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Haque A; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Aujla M; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Barrows R; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Beard D; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
  • Chandler C; Patient Representative, Norwich, UK.
  • Chandler E; Patient Representative, Norwich, UK.
  • Ellard DR; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Eldridge J; University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
  • Ferreira M; University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Foster NE; Sydney Musculoskeletal Health, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
  • Griffin J; STARS Education and Research Alliance, The University of Queensland and Metro North Health, Brisbane, Queensland, Australia.
  • Mason J; Keele University, Staffordshire, UK.
  • Mandalia V; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Parsons H; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Ray G; Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.
  • Stewart K; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Thompson P; University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
  • Underwood M; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Whitehouse MR; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Zanganeh M; University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
  • Metcalfe A; Warwick Clinical Trials Unit, University of Warwick, Coventry, UK.
  • Smith T; University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
BMJ Open ; 14(8): e090233, 2024 Aug 21.
Article em En | MEDLINE | ID: mdl-39174058
ABSTRACT

INTRODUCTION:

Recurrent patellar dislocation is a debilitating musculoskeletal condition, affecting mainly adolescents and adults under the age of 30. It can persist for many decades, causing pain and cartilage and soft-tissue damage, potentially leading to osteoarthritis. Recurrent patellar dislocation can be managed with physiotherapy or surgery. However, it is not known which treatment is most effective. METHODS AND

ANALYSIS:

Recurrent Patellar Dislocation Personalised Therapy or Operative Treatment (REPPORT) is a pragmatic, multicentre, two-arm, superiority, randomised controlled trial. It will compare the clinical and cost-effectiveness of an initial management strategy of personalised, phased and progressive rehabilitation, termed personalised knee therapy versus surgery for recurrent patellar dislocation.The trial's target sample size is 276 participants who will be recruited from approximately 20 sites across the UK. Participants will be randomly allocated to the two treatment groups via a central computer-based minimisation system. Treatment allocation will be in a 11 ratio, stratified by age, presence of patella alta and recruitment site.The primary outcome is participant-reported function using the Knee injury and Osteoarthritis Outcome 4-domain score at 18 months post randomisation. Health economic evaluation will be conducted from a healthcare system and personal social services perspective. Secondary outcome data including patellar instability, health utility, work/education status, satisfaction with social roles and treatment, health resource use and adverse events will be collected at 6, 12, 18 and 24 months. Analysis will be on an intention-to-treat basis and reported in-line with the Consolidated Standards of Reporting Trials statement. ETHICS AND DISSEMINATION The trial was approved by the East Midlands-Nottingham 2 Research Ethics Committee on 30 March 2023.Results will be disseminated via peer-reviewed publications, presentations at national and international conferences, in lay summaries, and using the REPPORT website and social media channels. TRIAL REGISTRATION NUMBER ISRCTN17972668.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Recidiva / Análise Custo-Benefício / Luxação Patelar Limite: Adolescent / Adult / Humans Idioma: En Revista: BMJ Open Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Recidiva / Análise Custo-Benefício / Luxação Patelar Limite: Adolescent / Adult / Humans Idioma: En Revista: BMJ Open Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido