Effect of Bracing Versus No Bracing in Stable Thoracolumbar Compression and Burst Fractures

NCT ID: NCT03952182

Last Updated: 2022-03-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

1 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-05

Study Completion Date

2022-03-22

Brief Summary

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Spinal orthoses have been used in the treatment of non-operative thoracic and lumbar fractures with much success. However, there has been increasing questioning as to wether or not the orthotics are necessary to have a good overall outcome. Being fitted for and acquiring braces are associated with great expense and increased hospital stays. The purpose of this study is to determine wether or not braces are required for good outcome post thoracic or lumbar fracture.

Detailed Description

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Several tens of patient's per year come to the Emergency Department with thoracolumbar spine compression and burst fractures that are not indicated for surgical fixation. Currently, these patients are treated non-operatively through brace wear which is either custom made for the patient or is off-the-shelf pending location of the fracture and surgeon preference. All braces are through the currently contracted orthotics company. As they are non stocked in house, waiting for the brace requires the patients to remain on "strict spine precautions" (flat bed rest in a Miami J collar, no pillows behind the head, and logrolls for turning) for anywhere from 24-48 hours. No only is this incredibly uncomfortable for the patient, it is also extending their hospital stay for at least one day and, sometimes, up to three as they wait for the brace and have it adjusted to fit appropriately. The patient's all have to then wait to work with physical therapy and occupational therapy and, finally, have upright spine films taken in the brace. The braces tend to be very uncomfortably and constricting for patient's and significantly inhibit their daily lives. The investigators are proposing that these fractures can be treated without needing bracewear and will have equivalent to superior outcomes than results while wearing the brace.

Conditions

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Thoracic Fracture Lumbar Fracture Compression Fracture of Thoracic Vertebral Body Compression Fracture of Lumbar Spine Burst Fracture of Thoracic Vertebra Burst Fracture of Lumbar Vertebra

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Spinal Orthosis (LSO, TLSO, etc)

Patient's in this arm will be given an orthosis for the treatment of their injury (TLSO for thoracic or upper lumbar injury, LSO for lumbar injury)

Group Type ACTIVE_COMPARATOR

Spinal Orthosis (LSO, TLSO)

Intervention Type OTHER

spinal orthosis prescribed for specific spinal fracture (TLSO for thoracic or high lumbar fracture, LSO for lumbar fracture)

No Spinal Orthosis

the patient's in this arm will not be given an orthotic. They will be given a bending restriction and otherwise remain activities as tolerated.

Group Type EXPERIMENTAL

No orthosis

Intervention Type OTHER

no orthotic given for spinal fracture. These patient's will be given a bending restriction

Interventions

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Spinal Orthosis (LSO, TLSO)

spinal orthosis prescribed for specific spinal fracture (TLSO for thoracic or high lumbar fracture, LSO for lumbar fracture)

Intervention Type OTHER

No orthosis

no orthotic given for spinal fracture. These patient's will be given a bending restriction

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Any acute, stable thoracic or lumbar compression or burst fracture appropriate for non-operative care

Exclusion Criteria

* neurological deficit, pregnant, incarcerated, non-English speaking, previous spinal surgery, additional lower extremity injury affecting weight bearing, younger than 18 years of age
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St. Louis University

OTHER

Sponsor Role lead

Responsible Party

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William Behrens, MD

Resident Physician

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Saint Louis University Hospital

St Louis, Missouri, United States

Site Status

Countries

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United States

Other Identifiers

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29976

Identifier Type: -

Identifier Source: org_study_id

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