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

被引:6
|
作者
Griffin, Xavier L. [1 ]
Costa, Matthew L. [1 ]
Achten, Juul [1 ]
Dritsaki, Melina [2 ]
Baird, Janis [3 ]
Parsons, Nicholas [4 ]
机构
[1] Univ Oxford, Kadoorie Ctr, NDORMS, OxfordTrauma, Oxford OX3 9DU, England
[2] Univ Oxford, NDORMS, Windmill Rd, Oxford OX3 7LD, England
[3] Univ Southampton, Southampton Gen Hosp, MRC Lifecourse Epidemiol Unit, Southampton SO16 6YD, Hants, England
[4] Univ Warwick, Warwick Med Sch, Stat & Epidemiol Unit, Coventry CV4 7AL, W Midlands, England
来源
TRIALS | 2017年 / 18卷
基金
美国国家卫生研究院;
关键词
Femur; Randomised controlled trial; Fracture fixation; QUALITY-OF-LIFE; DISTAL FEMUR; HIP FRACTURE; PEOPLE; EQ-5D; EPIDEMIOLOGY; DISABILITY; DEMENTIA; EUROQOL; DEMQOL;
D O I
10.1186/s13063-017-2265-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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 Muller 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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页数:8
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