- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03948139
Femur Fracture: Functional Bracing vs. Hip Spica Cast
Prospective Randomized Study Comparing Functional Bracing vs. Hip Spica Cast in Pediatric Femur Fractures
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Femur fractures are the most common orthopedic injury for which children are hospitalized in the United States. Traditional spica casts, the current standard of care for diaphyseal femoral shaft fractures with minimal shortening in children age 0-5 years old. Although spica cast immobilization is standard of care for femur fractures in young children, caring for a child in a spica cast presents a significant socioeconomic burden on families and the healthcare system. Basic hygiene and transportation for a child in a spica cast requires burdensome adjustments for caretakers, as well as the added expenses of specialized car seats or transportation services. Improper spica cast care can lead to skin complications, additional visits for cast adjustments, or even revision casting in the operating room.
Functional bracing plays an established role in the non-operative management of other long bone fractures in pediatric patients, and offers numerous advantages, including being lightweight, simple to apply, and conducive to hygienic skin care. A study conducted by Kramer et al. suggests there are both clinical and financial benefits of functional bracing when compared to spica casting for femur fractures, including increased patient/parent satisfaction and better cost effectiveness. To date, there have been no prospective trials to confirm these initial findings.
While previous work by Kramer et al demonstrated the advantages of functional bracing when compared to traditional spica casting, the ability to generalize this to other pediatric practices has been limited due to the challenges of making braces in a timely fashion. The braces utilized by Kramer et al require a carver to create a brace with a foot plate that improves rotational control for femur fractures. The cost of a carver is approximately $125,000, and thus few orthotists have access to this piece of equipment. This limits the ability for many pediatric orthopaedists to incorporate functional bracing into their practice.
To make this treatment option more cost effective and accessible, the investigators propose to generate five standardized sized braces based on measurements from prior scans that will be stocked at each institution and modified by the local orthoptist to fit the needs of each patient. This will facilitate expedited care while obtaining the same clinical and radiographic results as the fully customized braces. This idea has the potential to be extrapolated to the wider clinical community, creating a true shift in pediatric orthopaedic clinical practice throughout the country.
The investigators hypothesize that functional bracing will demonstrate equivalent objective outcomes with respect to leg length, time to union, rate of malunion, number of radiographs, and number of clinic visits. The investigators also hypothesize that functional bracing will demonstrate superior economic costs with respect to operating room cost and work days lost for parents, as well as subjective outcomes with respect to Pediatric Outcome Data Collection Instrument, patient/parent satisfaction.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tiffany N Phan, BA
- Phone Number: 323-361-2142
- Email: tphan@chla.usc.edu
Study Contact Backup
- Name: Kelleen Lopez, MPH
- Email: kelopez@chla.usc.edu
Study Locations
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California
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Los Angeles, California, United States, 90027
- Children's Hospital Los Angeles
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Colorado
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Aurora, Colorado, United States, 80045
- Children's Hospital Colorado
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients ages 0-5 years with an isolated diaphyseal femur fracture. Parents =18 years of age who are cognitively able to take a survey.
Exclusion Criteria:
- Patients >5 years of age without a diagnosis of an isolated diaphyseal femur fracture or polytrauma and those with medical co-morbidities that may affect fracture healing. Parents <18 year of age and unable to take a survey.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Functional Bracing Group
In a presented abstract, the functional brace group has been to shown equivalent outcomes to the hip spica cast.
Subject will be administered the functional brace without going to the operating room to be put under full anesthesia.
Most cases will not require any sedation in this group (in some cases, light sedation may be needed).
Brace will be used for up to 8 weeks post-administration, until adequate callous formation is confirmed.
|
The study will generate five standardized sized braces based on measurements from prior scans that will be stocked at each institution and modified by the local orthotist to fit the needs of each patient.
This will facilitate expedited care while obtaining the same clinical and radiographic results as the fully customized braces.
This idea has the potential to be extrapolated to the wider clinical community, creating a true shift in pediatric orthopaedic clinical practice throughout the country.
|
Other: Spica Cast Group
If subject is randomized into the hip spica cast group, subject will proceed to the operating room and be given general anesthesia to administer the spica cast.
Cast will be used for up to 8 weeks, until adequate callous formation is confirmed.
|
Traditional spica casts, the current standard of care for diaphyseal femoral shaft fractures with minimal shortening in children age 0-5 years old.
Although spica cast immobilization is standard of care for femur fractures in young children, caring for a child in a spica cast presents a significant socioeconomic burden on families and the healthcare system.
Basic hygiene and transportation for a child in a spica cast requires burdensome adjustments for caretakers, as well as the added expenses of specialized car seats or transportation services.
Improper spica cast care can lead to skin complications, additional visits for cast adjustments, or even revision casting in the operating room.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes in Leg Length
Time Frame: Radiographs will be reviewed at the pre-op and clinical follow-ups up to 1 year.
|
After treatment, leg length will be measured using clinical radiographs to determine if there are any changes to leg length and determine if there are discrepancies.
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Radiographs will be reviewed at the pre-op and clinical follow-ups up to 1 year.
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Changes in union/rate of malunion
Time Frame: Radiographs will be reviewed at the pre-op and clinical follow-ups up to 1 year.
|
This will be measuring the length of time and changes in union of bone, and to see if the bone has not healed properly.
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Radiographs will be reviewed at the pre-op and clinical follow-ups up to 1 year.
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Number of radiographs and clinic visits
Time Frame: This will be reviewed and counted for up to 1 year.
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This will be used to determine which arm had less radiation from radiographs and less visits with the surgeon.
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This will be reviewed and counted for up to 1 year.
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Economic costs (operating room cost)
Time Frame: This will be examined at the 1 day of intervention.
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This will be to compare the economic costs between the administration of a spica cast vs. a functional brace.
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This will be examined at the 1 day of intervention.
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Work days lost for parents
Time Frame: This will be surveyed at the 6 week post-intervention visit.
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This will be collected from a parent reported outcome survey which will help determine the amount of days a parent lost to work due to their child's condition.
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This will be surveyed at the 6 week post-intervention visit.
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Work days lost for parents
Time Frame: This will be surveyed at the 1 year post-intervention visit.
|
This will be collected from a parent reported outcome survey which will help determine the amount of days a parent lost to work due to their child's condition.
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This will be surveyed at the 1 year post-intervention visit.
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Pediatric Outcome Data Collection Instrument (PODCI)
Time Frame: This will be surveyed at the 6 week post-intervention visit.
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The PODCI is a validated quality of life and outcome questionnaire used for various pediatric orthopaedic studies.
It will allow the study team to determine the subjective outcomes of the subject.This will also be completed by the parent.
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This will be surveyed at the 6 week post-intervention visit.
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Pediatric Outcome Data Collection Instrument (PODCI)
Time Frame: This will be surveyed at the 1 year post-intervention visit.
|
The PODCI is a validated quality of life and outcome questionnaire used for various pediatric orthopaedic studies.
It will allow the study team to determine the subjective outcomes of the subject.This will also be completed by the parent.
|
This will be surveyed at the 1 year post-intervention visit.
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHLA-18-00233
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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