We aim to study the use of braces for thoracolumbar burstfractures, not only by measuring the functional scores and the effect of the bracing or functional treatment on the increase in kyphosis angle, but also on (health related) quality of life and…
ID
Bron
Verkorte titel
Aandoening
Spinal
Vertebral
Burstfracture
Orthesis
Spinaal
Wervel
Burstfractuur
Orthese/ brace
Ondersteuning
Postbus 90151
5000 LC Tilburg
Hilvarenbeekseweg 60
5022 GC Tilburg
Experiment Topzorg
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Function score (Oswestry Disability Index) 6 months after trauma.
Achtergrond van het onderzoek
Rationale: Thoracolumbar burst fractures are frequently seen in the trauma population, they have a large impact on patient’s wellbeing and are a large economic burden to society. Thoracolumbar burst fractures might not need the standard care of brace immobilization for adequate treatment and a functional treatment might lead to same or better functional outcomes. Besides that, with functional outcome length of hospital stay might decrease and it might also be cost effective compared to bracing.
Objective: We aim to study the use of braces for thoracolumbar burstfractures, not only by measuring the functional scores and the effect of the bracing or functional treatment on the increase in kyphosis angle, but also on (health related) quality of life and health economics. We hypothesize that no treatment is superior over one other by means of function, or pain.
Study design: This project is a randomised controlled trial comparing brace and no brace treatment on function, kyphosis angle, pain, QoL, and costs.
Study population: For the RCT patients between 18 and 65, with a single level thoracolumbar burst fracture will be included. The fracture has to have a kyphosis angle of less than 35 degrees and patient has to be neurologically intact. Patients are excluded when they are overweight (BMI> 35), need multidisciplinary treatment due to multitrauma, or have inadequate knowledge of the Dutch language. Patients included in the brace group will automatically take part in a brace compliance study.
Intervention: One group receives a Thoracolumbar Sacral Orthesis (TLSO) for 6 weeks, the other group receives no TLSO
Main study parameters/endpoints: The primary outcome of this study is the functional score at six months after trauma. Secondary outcomes are pain, kyphosis angle, health related quality of life, healthcare costs and brace compliance.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Literature shows no difference in pain, functional outcome or kyphosis angle, therefore no potential risks are known comparing a brace and a functional treatment. We aim that not using the TLSO results in similar functional outcome, pain and kyphosis angle, and less costs. Patients will be seen at first presentation and during two year follow up at the outpatient clinic at six standard care follow up moments. At these follow up moments a X-ray as part of standard care is made. At or just before each scheduled appointment they will fill in questionnaires taking from 15-45 minutes.
Doel van het onderzoek
We aim to study the use of braces for thoracolumbar burstfractures, not only by measuring the functional scores and the effect of the bracing or functional treatment on the increase in kyphosis angle, but also on (health related) quality of life and health economics. We hypothesize that no treatment is superior over one other by means of function, or pain.
Onderzoeksopzet
admission
1-2 weeks
6 weeks
3 months
6 months
1 year
2 years
Onderzoeksproduct en/of interventie
Subjects will wear a TLSO for 6 weeks 24 hours a day or they will not. The TLSO is customised and fitted on admission by the orthopaedic surgeon on call and/ or the supplier. After 6 weeks the subjects in the TLSO group will decrease and stop the use of the orthesis. Depending on their pain complaints patients will be admitted to the hospital and will get adequate pain management following local protocol.
Publiek
Wouter Bakker
Hilvarenbeekseweg 60 Postbus 90151
Tilburg 5000 LC
The Netherlands
013-5392942
bono@etz.nl
Wetenschappelijk
Wouter Bakker
Hilvarenbeekseweg 60 Postbus 90151
Tilburg 5000 LC
The Netherlands
013-5392942
bono@etz.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- 18-65 years
- Th10-L4
- AO type A3 or A4 type fractures
- Single level
- Kyphosis < 35 ° at first analysis
- Neurologically intact
- Adequate trauma
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Inadequate knowledge of the Dutch language
- Multitrauma, which asks for multidisciplinary treatment
- Inability to wear a brace due to overweight (BMI> 35)
- Known osteoporosis
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL4913 |
NTR-old | NTR5777 |
CCMO | NL55565.028.15 |
OMON | NL-OMON45936 |