Orthosis Versus no Orthosis After Dorsally Fixated Traumatic Thoracolumbar Fractures

Status: Recruiting
Location: See location...
Intervention Type: Other, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Age 18 - 65 years

• Traumatic thoracolumbar spine fracture from thoracic 7 - lumbar 4

• AO fracture types A-C

• Undergoing surgical dorsal fixation for fracture

Locations
Other Locations
Netherlands
VU University medical center
RECRUITING
Amsterdam
Contact Information
Primary
AJ Smits, MD
aj.smits@amsterdamumc.nl
Time Frame
Start Date: 2016-11
Estimated Completion Date: 2026-11
Participants
Target number of participants: 45
Treatments
Experimental: No orthosis
The intervention consists of a deviation of the standard protocol; patients post-operatively do not receive an orthosis.
Active_comparator: Orthosis
As in correspondence with local and international guidelines, patients receive an orthosis as standard post-operative care. This is considered the control group.
Related Therapeutic Areas
Sponsors
Leads: Amsterdam UMC, location VUmc

This content was sourced from clinicaltrials.gov