Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trial

Introduction Rotational malalignment occurs in up to 30% of cases after intramedullary nailing of tibial shaft fractures. The aim of this study is to assess the clinical feasibility of a newly introduced standardised intraoperative fluoroscopy protocol coined ‘C-arm rotational view (CARV)’ in order...

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Main Authors: Mostafa El Moumni, Job N Doornberg, Nils Jan Bleeker, Kaj ten Duis, Ruurd L Jaarsma, Frank F A IJpma
Format: Article
Language:English
Published: BMJ Publishing Group 2023-11-01
Series:BMJ Open
Online Access:https://bmjopen.bmj.com/content/13/11/e064802.full
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author Mostafa El Moumni
Job N Doornberg
Nils Jan Bleeker
Kaj ten Duis
Ruurd L Jaarsma
Frank F A IJpma
author_facet Mostafa El Moumni
Job N Doornberg
Nils Jan Bleeker
Kaj ten Duis
Ruurd L Jaarsma
Frank F A IJpma
author_sort Mostafa El Moumni
collection DOAJ
description Introduction Rotational malalignment occurs in up to 30% of cases after intramedullary nailing of tibial shaft fractures. The aim of this study is to assess the clinical feasibility of a newly introduced standardised intraoperative fluoroscopy protocol coined ‘C-arm rotational view (CARV)’ in order to reduce the risk of rotational malalignment during intramedullary nailing of tibial shaft fractures. The CARV includes predefined fluoroscopy landmark views of the uninjured side to obtain correct alignment of the injured side with use of the rotation of the C-arm.Methods and analysis This randomised controlled trial will be conducted in a level 1 trauma centre. Adult patients with an open or closed tibial fracture, eligible for intramedullary nailing, will be enrolled in the study. The interventional group will undergo intramedullary nailing guided by the CARV protocol to obtain accurate alignment. The control group is treated according to current clinical practice, in which alignment control of the tibia is based on clinical estimation of the treating surgeon. The primary endpoint is defined as the degree of rotation measured on low-dose postoperative CT scans.Ethics and dissemination The study protocol will be performed in line with local ethical guidelines and the Declaration of Helsinki. The results of this trial will be disseminated in a peer-reviewed manuscript. Future patients are likely to benefit from this trial as it aims to provide a clinically feasible and easy-to-use standardised fluoroscopy protocol to reduce the risk for rotational malalignment during intramedullary nailing of tibial shaft fractures.Trial registration number NCT05459038.
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spelling doaj.art-5afba0d78c964984b509db5f45051c562023-12-01T23:40:07ZengBMJ Publishing GroupBMJ Open2044-60552023-11-01131110.1136/bmjopen-2022-064802Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trialMostafa El Moumni0Job N Doornberg1Nils Jan Bleeker2Kaj ten Duis3Ruurd L Jaarsma4Frank F A IJpma5Orthopaedic Trauma Surgery, University Medical Centre Groningen, Groningen, The NetherlandsOrthopaedic Trauma Surgery, University Medical Centre Groningen, Groningen, The NetherlandsOrthopaedic Trauma Surgery, University Medical Centre Groningen, Groningen, The NetherlandsOrthopaedic Trauma Surgery, University Medical Centre Groningen, Groningen, The NetherlandsOrthopaedic Trauma Surgery, Flinders Medical Centre, Bedford Park, South Australia, AustraliaOrthopaedic Trauma Surgery, Universitair Medisch Centrum Groningen, Groningen, The NetherlandsIntroduction Rotational malalignment occurs in up to 30% of cases after intramedullary nailing of tibial shaft fractures. The aim of this study is to assess the clinical feasibility of a newly introduced standardised intraoperative fluoroscopy protocol coined ‘C-arm rotational view (CARV)’ in order to reduce the risk of rotational malalignment during intramedullary nailing of tibial shaft fractures. The CARV includes predefined fluoroscopy landmark views of the uninjured side to obtain correct alignment of the injured side with use of the rotation of the C-arm.Methods and analysis This randomised controlled trial will be conducted in a level 1 trauma centre. Adult patients with an open or closed tibial fracture, eligible for intramedullary nailing, will be enrolled in the study. The interventional group will undergo intramedullary nailing guided by the CARV protocol to obtain accurate alignment. The control group is treated according to current clinical practice, in which alignment control of the tibia is based on clinical estimation of the treating surgeon. The primary endpoint is defined as the degree of rotation measured on low-dose postoperative CT scans.Ethics and dissemination The study protocol will be performed in line with local ethical guidelines and the Declaration of Helsinki. The results of this trial will be disseminated in a peer-reviewed manuscript. Future patients are likely to benefit from this trial as it aims to provide a clinically feasible and easy-to-use standardised fluoroscopy protocol to reduce the risk for rotational malalignment during intramedullary nailing of tibial shaft fractures.Trial registration number NCT05459038.https://bmjopen.bmj.com/content/13/11/e064802.full
spellingShingle Mostafa El Moumni
Job N Doornberg
Nils Jan Bleeker
Kaj ten Duis
Ruurd L Jaarsma
Frank F A IJpma
Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trial
BMJ Open
title Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trial
title_full Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trial
title_fullStr Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trial
title_full_unstemmed Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trial
title_short Clinical validation of the ‘C-arm rotational view (CARV)’: study protocol of a prospective randomised controlled trial
title_sort clinical validation of the c arm rotational view carv study protocol of a prospective randomised controlled trial
url https://bmjopen.bmj.com/content/13/11/e064802.full
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