LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trial

Introduction Open reduction and internal fixation with volar locking plate has become the most common fixation method in the treatment of unstable distal radius fracture (DRF). There is, however, no consensus as to whether or for how long a wrist should be immobilised after operative treatment. To d...

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Main Authors: Teemu Karjalainen, Antti P Launonen, Ville M Mattila, Ville Ponkilainen, Aleksi Reito, Mika Helminen, Toni Luokkala, Laura Kärnä, Lauri Halonen
Format: Article
Language:English
Published: BMJ Publishing Group 2022-11-01
Series:BMJ Open
Online Access:https://bmjopen.bmj.com/content/12/11/e064440.full
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author Teemu Karjalainen
Antti P Launonen
Ville M Mattila
Ville Ponkilainen
Aleksi Reito
Mika Helminen
Toni Luokkala
Laura Kärnä
Lauri Halonen
author_facet Teemu Karjalainen
Antti P Launonen
Ville M Mattila
Ville Ponkilainen
Aleksi Reito
Mika Helminen
Toni Luokkala
Laura Kärnä
Lauri Halonen
author_sort Teemu Karjalainen
collection DOAJ
description Introduction Open reduction and internal fixation with volar locking plate has become the most common fixation method in the treatment of unstable distal radius fracture (DRF). There is, however, no consensus as to whether or for how long a wrist should be immobilised after operative treatment. To date, there have been relatively few studies that have evaluated the effect of immediate postoperative mobilisation on functional outcomes. The aim of postoperative rehabilitation is to obtain a good function and to reduce impairment, recovery time, socioeconomical costs and absence from work. Therefore, there is a need for studies that evaluate the optimal method of postoperative rehabilitation to optimise wrist function and return to work.Methods and analysis This study is a prospective, randomised, controlled trial in which a total of 240 working-age patients who undergo volar plating for DRF will be randomly assigned to either an early mobilisation group or a postoperative 2-week casting group. The aim of the study will be to compare early postoperative outcomes between the study groups. The primary outcome will be patient-rated wrist evaluation at 2 months after operation. A coprimary outcome will be the total length of sick leave. Our follow-up period will be 1 year, and secondary outcomes will include pain, patient satisfaction, perceived ability to work and complications identified at different time points. We expect those patients who undergo immediate mobilisation will have at least as rapid a return to work and function as those patients who undergo postoperative immobilisation, indicating/meaning that there will be no need for postoperative casting.Ethics and dissemination This study will be conducted according to the Standard Protocol Items: Recommendations for Interventional Trials statement. The Ethics committee of Tampere University Hospital has approved the protocol. Ethics committee approval number is R21111, and it is accepted on 7 September 2021. The results of this study will be submitted for publication in peer-reviewed journals.Trial registration number NCT05150925.
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spelling doaj.art-8fd6ae27a5b84cbab2d090140111c7822022-12-22T04:13:50ZengBMJ Publishing GroupBMJ Open2044-60552022-11-01121110.1136/bmjopen-2022-064440LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trialTeemu Karjalainen0Antti P Launonen1Ville M Mattila2Ville Ponkilainen3Aleksi Reito4Mika Helminen5Toni Luokkala6Laura Kärnä7Lauri Halonen8Central Finland Central Hospital, Jyvaskyla, FinlandTampere University Hospital, Tampere, FinlandTampere University Hospital, Tampere, FinlandCentral Finland Central Hospital, Jyvaskyla, FinlandTampere University Hospital, Tampere, FinlandHealth Sciences, Research Services, Tampere, FinlandCentral Finland Central Hospital, Jyvaskyla, FinlandTampere University Hospital, Tampere, FinlandSouth Karelia Central Hospital, Lappeenranta, FinlandIntroduction Open reduction and internal fixation with volar locking plate has become the most common fixation method in the treatment of unstable distal radius fracture (DRF). There is, however, no consensus as to whether or for how long a wrist should be immobilised after operative treatment. To date, there have been relatively few studies that have evaluated the effect of immediate postoperative mobilisation on functional outcomes. The aim of postoperative rehabilitation is to obtain a good function and to reduce impairment, recovery time, socioeconomical costs and absence from work. Therefore, there is a need for studies that evaluate the optimal method of postoperative rehabilitation to optimise wrist function and return to work.Methods and analysis This study is a prospective, randomised, controlled trial in which a total of 240 working-age patients who undergo volar plating for DRF will be randomly assigned to either an early mobilisation group or a postoperative 2-week casting group. The aim of the study will be to compare early postoperative outcomes between the study groups. The primary outcome will be patient-rated wrist evaluation at 2 months after operation. A coprimary outcome will be the total length of sick leave. Our follow-up period will be 1 year, and secondary outcomes will include pain, patient satisfaction, perceived ability to work and complications identified at different time points. We expect those patients who undergo immediate mobilisation will have at least as rapid a return to work and function as those patients who undergo postoperative immobilisation, indicating/meaning that there will be no need for postoperative casting.Ethics and dissemination This study will be conducted according to the Standard Protocol Items: Recommendations for Interventional Trials statement. The Ethics committee of Tampere University Hospital has approved the protocol. Ethics committee approval number is R21111, and it is accepted on 7 September 2021. The results of this study will be submitted for publication in peer-reviewed journals.Trial registration number NCT05150925.https://bmjopen.bmj.com/content/12/11/e064440.full
spellingShingle Teemu Karjalainen
Antti P Launonen
Ville M Mattila
Ville Ponkilainen
Aleksi Reito
Mika Helminen
Toni Luokkala
Laura Kärnä
Lauri Halonen
LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trial
BMJ Open
title LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trial
title_full LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trial
title_fullStr LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trial
title_full_unstemmed LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trial
title_short LIMPER trials: immediate mobilisation versus 2-week cast immobilisation after distal radius fracture treated with volar locking plate – a study protocol for a prospective, randomised, controlled trial
title_sort limper trials immediate mobilisation versus 2 week cast immobilisation after distal radius fracture treated with volar locking plate a study protocol for a prospective randomised controlled trial
url https://bmjopen.bmj.com/content/12/11/e064440.full
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