Fracture Clinical Trial
Official title:
A Randomised Controlled Trial of Outcome of Different Post Operative Rehabilitation Regime Following Internally Fixed Ankle Fractures
The purpose of this study is to examine the effect of variations in practice, ranging from
early functional rehabilitation to complete immobilsation in post operative patients with
ankle fixation following fractures. The primary goal of any post-operative regimen is to
attain full weight-bearing and as close to pre-injury levels of activity as soon as
possible.
We seek to establish the effect on (1) functional outcome, (2) complication rates and (3)
time to return to work of three different approaches to rehabilitation after ankle fracture
fixation in order to produce a standardised, evidence-based guideline for our unit. We also
aim to perform a cost analysis for each approach.
Although the indications for fixation of an ankle fracture are relatively clear, controversy
exists with regards the post-operative management of these fractures.
This is a prospective randomised controlled trial. All patients admitted to the Countess of
Chester NHS Foundation Trust Orthopaedic Unit for ankle fracture fixation who met the set
study inclusion criteria will be given a patient information pack regarding the trial and
asked to complete a consent form to enter the trial AFTER their operation has been
performed. All patients will initially have their ankle immobilised in a below knee backslab
applied in theatre and reviewed at 2 weeks in the plaster room for removal of plaster and
sutures. At this setting the patient will be randomised to 1 of 3 rehabilitation arms using
a sealed envelope technique. All patients data will be anonymised following generation of a
randomisation number.
3 Orthopaedic Consultants (JH,KT,EW) will thereafter supervise follow-up of the study
population until discharge at 1 year. Outcome measures recorded include patient -reported
functional scores (MOxFQ); clinical assessment of range of motion, complication rates (loss
of reduction); pain scores, satisfaction rates and return to work. Clinic review organised
at 2 weeks for randomisation, 6 weeks for first post-op xrays and removal of plaster/ brace,
8 weeks for clinical review specifically range of movement achievable at ankle, 3 months
with repeat Xray and clinical assessment, and final clinical review in clinic at 6 months in
the fracture clinic. Telephone/ postal questionnaire to gather MoXFQ scores at 1 year.
There are no ethical or legal issues related to the studies.
One potential concern will be loss of reduction and fixation of ankle fractures following
weight bearing without immobilisation. However, a study published by Gul et al in 2007
relating to immediate weight-bearing of operatively treated ankle fractures without
immobilisation in cast showed no evidence of loss of reduction or hardware failure compared
to historical controls.
Patients will be reviewed closely in the early period for loss of reduction as a safety
outcome measure and the result will be monitored closely with earlier termination of trial
should there be a concern. There will be monthly data review and monitoring during a
research meeting.
Reference
Gul AG, Batra S, Meehmood S, Gillham N. Immediate unprotected weight-bearing of operatively
treated ankle fractures. Acta Orthop Belgica 2007;73:360-365.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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