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ORthosis vs No Orthosis After Surgically Treated Traumatic Thoracolumbar Fractures (ORNOT)

Primary Purpose

Spine Fracture, Orthosis, Traumatic Fracture

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
No orthosis
Orthosis
Sponsored by
Amsterdam UMC, location VUmc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spine Fracture

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 - 65 years
  • Traumatic thoracolumbar spine fracture from thoracic 7 - lumbar 4
  • AO fracture types A-C
  • Undergoing surgical dorsal fixation for fracture

Exclusion Criteria:

  • 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
  • Not able to walk before fracturing vertebra
  • Unable to come to the outpatient clinic (e.g. residing outside the Netherlands)
  • Injury Severity Score (ISS) ≥ 16
  • Brain injury with Abbreviated Injury Score (AIS) ≥ 4
  • Solitary Lumbar 5 fracture
  • Inability to wear an orthosis, most probable reasons:

    • BMI > 35
    • Thoraco-abdominal wounds (through trauma or secondary from surgery) on places at which the orthosis contacts the body so aggravation of pain or chances of infection increase significantly.

      12 of 27

    • Pre-existing spine deformities (scoliosis or very severe kyphosis/lordosis) which impair the use of the orthosis or aggravate pain.

Sites / Locations

  • VU University medical centerRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

No orthosis

Orthosis

Arm Description

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

As in correspondence with local and international guidelines, patients receive an orthosis as standard post-operative care. This is considered the control group.

Outcomes

Primary Outcome Measures

Pain (NRS)

Secondary Outcome Measures

Pain (NRS)
Quality of life (EQ-5D)
Back pain related function (ODI)
Kyphosis (Cobb-angle)

Full Information

First Posted
March 20, 2017
Last Updated
January 21, 2023
Sponsor
Amsterdam UMC, location VUmc
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1. Study Identification

Unique Protocol Identification Number
NCT03097081
Brief Title
ORthosis vs No Orthosis After Surgically Treated Traumatic Thoracolumbar Fractures
Acronym
ORNOT
Official Title
Orthosis Versus no Orthosis After Dorsally Fixated Traumatic Thoracolumbar Fractures
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 2016 (undefined)
Primary Completion Date
January 2025 (Anticipated)
Study Completion Date
November 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Amsterdam UMC, location VUmc

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spine Fracture, Orthosis, Traumatic Fracture, Posterior Fixation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
No orthosis
Arm Type
Experimental
Arm Description
The intervention consists of a deviation of the standard protocol; patients post-operatively do not receive an orthosis.
Arm Title
Orthosis
Arm Type
Active Comparator
Arm Description
As in correspondence with local and international guidelines, patients receive an orthosis as standard post-operative care. This is considered the control group.
Intervention Type
Other
Intervention Name(s)
No orthosis
Intervention Description
The intervention consists of a deviation of the standard protocol; patients do not receive a post-operative orthosis
Intervention Type
Device
Intervention Name(s)
Orthosis
Intervention Description
Patients receive post-operative care following the standard protocol and wear an orthosis for 10-12 weeks.
Primary Outcome Measure Information:
Title
Pain (NRS)
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Pain (NRS)
Time Frame
Post-operative, 2 & 12 weeks
Title
Quality of life (EQ-5D)
Time Frame
Post-operative, 12 weeks & 6, 12 months
Title
Back pain related function (ODI)
Time Frame
Post-operative, 2, 6, 12 weeks & 6, 12 months
Title
Kyphosis (Cobb-angle)
Time Frame
Pre-operative, post-operative, 6, 12 weeks & 6, 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 - 65 years Traumatic thoracolumbar spine fracture from thoracic 7 - lumbar 4 AO fracture types A-C Undergoing surgical dorsal fixation for fracture Exclusion Criteria: 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 Not able to walk before fracturing vertebra Unable to come to the outpatient clinic (e.g. residing outside the Netherlands) Injury Severity Score (ISS) ≥ 16 Brain injury with Abbreviated Injury Score (AIS) ≥ 4 Solitary Lumbar 5 fracture Inability to wear an orthosis, most probable reasons: BMI > 35 Thoraco-abdominal wounds (through trauma or secondary from surgery) on places at which the orthosis contacts the body so aggravation of pain or chances of infection increase significantly. 12 of 27 Pre-existing spine deformities (scoliosis or very severe kyphosis/lordosis) which impair the use of the orthosis or aggravate pain.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
AJ Smits, MD
Email
aj.smits@amsterdamumc.nl
Facility Information:
Facility Name
VU University medical center
City
Amsterdam
State/Province
Noord-Holland
ZIP/Postal Code
1018HV
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
AJ Smits, MD
Email
aj.smits@vumc.nl
First Name & Middle Initial & Last Name & Degree
FW Bloemers, MD, PhD
First Name & Middle Initial & Last Name & Degree
J Deunk, MD, PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
29331975
Citation
Smits AJ, Deunk J, Stadhouder A, Altena MC, Kempen DHR, Bloemers FW. Is postoperative bracing after pedicle screw fixation of spine fractures necessary? Study protocol of the ORNOT study: a randomised controlled multicentre trial. BMJ Open. 2018 Jan 13;8(1):e019596. doi: 10.1136/bmjopen-2017-019596.
Results Reference
derived

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ORthosis vs No Orthosis After Surgically Treated Traumatic Thoracolumbar Fractures

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