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Trial of Acute Femoral Fracture Fixation (TrAFFix): study protocol for a randomised controlled feasibility trial

Trial of Acute Femoral Fracture Fixation (TrAFFix): study protocol for a randomised controlled feasibility trial
Trial of Acute Femoral Fracture Fixation (TrAFFix): study protocol for a randomised controlled feasibility trial
Background: distal femoral fractures are a source of considerable morbidity and best treatment is currently uncertain. The Trial of Acute Femoral Fracture Fixation (TrAFFix) is a randomised, parallel-group feasibility study designed to inform the design of a later, definitive clinical trial comparing intramedullary nails and locking plates for the treatment of distal femoral fractures.

Methods/design: patients aged 50 years and older with a femoral fracture within the distal two Müller squares are potentially eligible for inclusion. Participants are randomly allocated to receive fixation with either an intramedullary nail or a distal locking plate. Measurements (EuroQol 5 Dimensions, Dementia Quality of Life, Disability Rating Index) are collected at baseline, 6 weeks and 4 months. The recruitment rate will be assessed across seven participating centres over a total of 52 centre-months which is expected after 10 months of recruitment. Objectives are – feasibility phase, to assess recruitment rate and completion rate of the primary outcome measure; process evaluation, to assess the generalisability and likely success of a future trial; definitive trial, quantify and draw inferences on observed differences in health-related quality of life at 4 months between the study intervention groups (nail versus plate). A favourable opinion was granted by the Wales Research Ethics Committee (16/WA/0225), study-wide NHS approval was given by the Health Research Authority (IRAS 206745), and participating NHS trusts provided local approvals. This study was funded by the National Institute for Health Research Health Technology Assessment (HTA 15/59/22).

Discussion: this is the protocol for a feasibility study conducted prior to any future definitive trial. The estimates of participant recruitment rate and proportion of data completion will be coupled with outputs from the process evaluation to make a final decision regarding feasibility

1745-6215
538
Griffin, X L
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Costa, M.L.
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Achten, J
302b6489-d0fe-433f-abe1-ce9d454308e5
Dritsaki, M.
d2ac5527-171e-4aa1-a692-d6c10a327f8a
Baird, Janis
f4bf2039-6118-436f-ab69-df8b4d17f824
Parsons, N.
5317e3ff-2f13-40ac-af03-a0e9895a4abc
Griffin, X L
bca543c1-d03f-4b73-8e29-842c4b4f3667
Costa, M.L.
49159f2e-f22f-406b-905c-a0e81f5f70d5
Achten, J
302b6489-d0fe-433f-abe1-ce9d454308e5
Dritsaki, M.
d2ac5527-171e-4aa1-a692-d6c10a327f8a
Baird, Janis
f4bf2039-6118-436f-ab69-df8b4d17f824
Parsons, N.
5317e3ff-2f13-40ac-af03-a0e9895a4abc

Griffin, X L, Costa, M.L., Achten, J, Dritsaki, M., Baird, Janis and Parsons, N. (2017) Trial of Acute Femoral Fracture Fixation (TrAFFix): study protocol for a randomised controlled feasibility trial. Trials, 18, 538. (doi:10.1186/s13063-017-2265-0).

Record type: Article

Abstract

Background: distal femoral fractures are a source of considerable morbidity and best treatment is currently uncertain. The Trial of Acute Femoral Fracture Fixation (TrAFFix) is a randomised, parallel-group feasibility study designed to inform the design of a later, definitive clinical trial comparing intramedullary nails and locking plates for the treatment of distal femoral fractures.

Methods/design: patients aged 50 years and older with a femoral fracture within the distal two Müller squares are potentially eligible for inclusion. Participants are randomly allocated to receive fixation with either an intramedullary nail or a distal locking plate. Measurements (EuroQol 5 Dimensions, Dementia Quality of Life, Disability Rating Index) are collected at baseline, 6 weeks and 4 months. The recruitment rate will be assessed across seven participating centres over a total of 52 centre-months which is expected after 10 months of recruitment. Objectives are – feasibility phase, to assess recruitment rate and completion rate of the primary outcome measure; process evaluation, to assess the generalisability and likely success of a future trial; definitive trial, quantify and draw inferences on observed differences in health-related quality of life at 4 months between the study intervention groups (nail versus plate). A favourable opinion was granted by the Wales Research Ethics Committee (16/WA/0225), study-wide NHS approval was given by the Health Research Authority (IRAS 206745), and participating NHS trusts provided local approvals. This study was funded by the National Institute for Health Research Health Technology Assessment (HTA 15/59/22).

Discussion: this is the protocol for a feasibility study conducted prior to any future definitive trial. The estimates of participant recruitment rate and proportion of data completion will be coupled with outputs from the process evaluation to make a final decision regarding feasibility

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Accepted/In Press date: 21 October 2017
e-pub ahead of print date: 14 November 2017

Identifiers

Local EPrints ID: 417735
URI: http://eprints.soton.ac.uk/id/eprint/417735
ISSN: 1745-6215
PURE UUID: 9fe8ac34-3078-49f7-85fe-272d78a08a59
ORCID for Janis Baird: ORCID iD orcid.org/0000-0002-4039-4361

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Date deposited: 12 Feb 2018 17:30
Last modified: 16 Mar 2024 03:29

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Contributors

Author: X L Griffin
Author: M.L. Costa
Author: J Achten
Author: M. Dritsaki
Author: Janis Baird ORCID iD
Author: N. Parsons

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