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Non-operative Treatment of Pediatric Lateral Humeral Condyle Fractures

Non-operative Treatment of Pediatric Lateral Humeral Condyle Fractures: a Cohort Study of 50 Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05096689
Acronym
NOTICE
Enrollment
50
Registered
2021-10-27
Start date
2021-11-01
Completion date
2024-10-01
Last updated
2021-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fracture Humerus, Physeal Fracture

Brief summary

The diagnosis of LHCF is complicated by radiographic inability to show the full extent of the injury into the chondral (unossified) epiphysis. MRI gives a perfect view of these fractures. The safety and feasibility of non-operative treatment based on MRI findings in children with elbow fractures has not been investigated in a Danish setting. If safe and feasible, the use of MRI could dramatically lower the need for surgery in children with LHCF.

Detailed description

The treatment of LHCF has historically most often been surgical with open reduction and fixation. The diagnosis of LHCF is complicated by radiographic inability to show the full extent of the injury into the unossified chondral epiphysis and therefore physicians often opt for open surgical treatment. MRI; however, gives a perfect view of these fractures. This project investigates the safety and feasibility of non-operative treatment of LHCF based on MRI performed without sedation or anesthesia and seeks to dramatically lower the need for surgery. Objectives are to describe functional outcome, radiological healing, secondary fracture displacement and any complications after two years. The investigators hypothesize that undisplaced and minimally displaced LHCF can be treated non-operatively based on MRI findings with good functional outcomes after two years. A cohort study design is used to follow 50 children with LHCF.

Interventions

OTHERMRI

Magnetic Resonance Imaging

Sponsors

Children's Fractures Interest Group, Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Prospective, Cohort, Single center

Eligibility

Sex/Gender
ALL
Age
2 Years to 13 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of acute Lateral humeral condyle fracture * Fracture \<5 days old * Fracture with \<5 mm of displacement on plain radiographs * Parental informed consent obtained

Exclusion criteria

* Contraindication(s) to performing an MRI * Unable to participate in follow-up * Existing bone pathology * Previous ipsilateral elbow fracture

Design outcomes

Primary

MeasureTime frameDescription
Mayo Elbow Performance Score (MEPS)2 yearsMEPS consists of three domains; pain, elbow range of motion (ROM) and stability. The total score ranges from 0-100 with higher scores indicating better function. If the total score ranges between 75 and 100, the result is good (satisfactory); 50-74, fair (acceptable); \<50, poor (unsatisfactory).

Secondary

MeasureTime frameDescription
Radiographic results2 yearsInjury radiographs and subsequent radiographs during FU will be read and described by a senior orthopedic surgeon.
Secondary fracture displacement2 yearsAny secondary displacement and amount of radiographic displacement (mm) is recorded.
MRI results2 weeksProportion of successful MRIs defined as a completed scan with an image quality that is useful for analysis by the radiologist. MRI findings. Song classification based on MRI. Scan length (minutes). Any discomforts for the child during the scan.
Pain scale (age >4 years)2 yearsTo quantify pain in the patient \>4 years, Faces Pain Scale - Revised (FPS-R) is applied. The Faces Pain Scale - Revised (FPS-R) is used to quantify pain in children above four years of age. It is a self-report measure of pain intensity developed for children. It was adapted from the Faces Pain Scale to make it possible to score the sensation of pain on a 0-to-10 metric. The scale shows a close linear relationship with visual analog pain scales (VAS) across the age range of 4-16 years. FPS-R is easy to administer and requires no equipment except for the photocopied faces. The child is asked to point to the face that shows how much pain the child is in at that moment. Faces are scored 0-10 so 0 equals no pain and 10 equals very much pain.
Pain scale (age >8 years)2 yearsA visual analogue scale (VAS) is used to quantify pain in children age 8 and above. VAS has been extensively investigated in quantifying pain in older children. The child is asked to put a mark on the line corresponding to the child's pain at that moment. A mark to the far left equals no pain and a mark to the far right equals worst possible pain. The line is 10 cm long and the child's mark is measured from left to right in cm with one decimal e.g., 3.4 cm equaling a VAS of 3.4. If the child cannot cooperate to using VAS, FPS-R is used instead.
Pain scale (age <5 years)2 yearsTo quantify pain in the patient age \<5 years, the Face, Legs, Activity, Cry, Consolability Scale (FLACC). To quantify pain behaviors in children who may not be able to verbalize the presence or severity of pain FLACC provides a simple framework. The child is observed for at least 2-5 minutes. Legs and body are observed uncovered. Activity is observed and body is assessed for tenseness and tone. Assessment of Behavioural Score: 0 = Relaxed and comfortable. 1-3 = Mild discomfort. 4-6 = Moderate pain. 7-10 = Severe discomfort/pain.

Countries

Denmark

Contacts

Primary ContactMorten J Andersen, MD
mortenjonandersen@gmail.com004538681479

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026