ORthosis vs No Orthosis After Surgically Treated Traumatic Thoracolumbar Fractures

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAmsterdam UMC, location VUmc

About this trial

Rationale: There is no evidence in the current literature regarding the additional value of an orthosis after surgically treated thoracolumbar spine fractures.

Objective: To assess whether an orthosis provides additional pain relief compared to no orthosis after posteriorly fixated thoracolumbar spine fractures. Primary outcome is difference in pain at six weeks post-operatively. Secondary objectives are pain at other moments, pain medication used, pain related disability, quality of life, long-term kyphosis, possible complications, hospital stay, return to work and subjective feeling on benefit or disadvantage from the orthosis.

Study design: Randomized controlled intervention study, non-inferiority trial.

Study population: Dutch speaking patients presented at the VU university medical centre, 18 - 65 years old with a traumatic thoracolumbar spine fracture from Th7 - L4 surgically treated by posterior fixation.

Intervention: One group receives standard care and wears an orthosis after surgery for 12 weeks, to use when in vertical position. The intervention group does not wear an orthosis after surgery.

Main study parameters/endpoints: Main study outcome is the difference in pain noted on the NRS-score at six weeks, ≥ 2 (SD 2,5) change corresponds with a clinically significant change in pain score.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The current guideline for postoperative care regarding dorsal stabilization of spine fractures recommends the use of a post-operative orthosis. While patients generally receive an orthosis for 12 weeks, individual surgeon's believes sometimes gives reason to deviate from this guideline. This is founded by literature that increasingly questions the use of orthoses in the conservative treatment of spine fractures. With the fracture operatively stabilized, the orthosis mainly provides support of gesture and thereby potentially results in pain relief and confidence for patients. On the other hand some patients have a hard time weaning from the orthosis or report discomfort due to the device and prefer not to use it. With subjects being randomized between the use of an orthosis or no orthosis there is no additional risk. This is in part because it is hypothesized that there is no difference in postoperative pain and there might be a lower risk of complications related to the orthosis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 - 65 years

Traumatic thoracolumbar spine fracture from thoracic 7 - lumbar 4

AO fracture types A-C

Undergoing surgical dorsal fixation for fracture

Disqualifiers

Inadequate knowledge of Dutch language or to fill in questionnaire

Complete or partial spinal cord injury (ASIA A to D)

(Additional) anterior surgical stabilization

Thoracolumbar fracture of other aetiology than traumatic, e.g. pathologic, infectious

Trial design

Design model

Parallel

Treatments tested in this trial

  • No orthosis

    Other intervention

    The intervention consists of a deviation of the standard protocol; patients do not receive a post-operative orthosis

  • Orthosis

    Device

    Patients receive post-operative care following the standard protocol and wear an orthosis for 10-12 weeks.

Treatment groups

45 Participants
are divided into 2 treatment groups
Group A: No orthosisExperimental treatment 1 intervention
Group B: OrthosisActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain (NRS)

Time frame
6 weeks

Secondary outcomes

1

Pain (NRS)

Time frame
Post-operative, 2 & 12 weeks
2

Quality of life (EQ-5D)

Time frame
Post-operative, 12 weeks & 6, 12 months
3

Back pain related function (ODI)

Time frame
Post-operative, 2, 6, 12 weeks & 6, 12 months
4

Kyphosis (Cobb-angle)

Time frame
Pre-operative, post-operative, 6, 12 weeks & 6, 12 months

Other outcomes

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