VU University medical center
Amsterdam, North Holland, 1018HV, Netherlands
Location status: Recruiting
Location contact
AJ Smits, MD
CONTACT
FW Bloemers, MD, PhD
PRINCIPAL_INVESTIGATOR
J Deunk, MD, PhD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT03097081
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.
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Not applicable
Amsterdam, North Holland, 1018HV, Netherlands
Location status: Recruiting
AJ Smits, MD
CONTACT
FW Bloemers, MD, PhD
PRINCIPAL_INVESTIGATOR
J Deunk, MD, PhD
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
12 of 27
The intervention consists of a deviation of the standard protocol; patients do not receive a post-operative orthosis
Patients receive post-operative care following the standard protocol and wear an orthosis for 10-12 weeks.
Time frame: 6 weeks
Time frame: Post-operative, 2 & 12 weeks
Time frame: Post-operative, 12 weeks & 6, 12 months
Time frame: Post-operative, 2, 6, 12 weeks & 6, 12 months
Time frame: Pre-operative, post-operative, 6, 12 weeks & 6, 12 months
Contact information is provided by the study sponsor or research team.
Amsterdam UMC, location VUmc
Other
Orthosis Versus no Orthosis After Dorsally Fixated Traumatic Thoracolumbar Fractures
Acronym: ORNOT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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