Multi-Center Adolescent Clavicle Fracture Trial: Operative vs. Non-Operative Treatment

  • STATUS
    Recruiting
  • participants needed
    250
  • sponsor
    Boston Children’s Hospital
Updated on 19 February 2024

Summary

Investigators from eight tertiary care, level 1 pediatric trauma centers have developed a protocol for the establishment of a formal, prospective multi-center adolescent clavicle registry, with designs for standardized radiographic assessment and the prospective collection of validated outcome measures and complications data, for all patients, ages 10-18, treated for clavicle shaft fractures, operatively and non-operatively. Eventually, the investigators would like to do comparative analysis for the operative and non-operative treatment arms, with additional sub-stratified analyses performed within these treatment arms by age and activity level. Among the primary goals of research projects stemming from the first arm of this registry, FACTS A, is to explore the hypothesis that non-operative treatment is associated with lower costs, greater safety, and equivalent or superior outcomes, compared with operative treatment, despite a national trend towards increasing surgical treatment. The second arm of the registry, FACTS B, will continue to investigate the same hypotheses, excluding cost outcomes, in patients only with completely displaced midshaft clavicle fractures.

Details
Condition Clavicle Fracture
Age 10-18 years
Treatment Surgery
Clinical Study IdentifierNCT04250415
SponsorBoston Children’s Hospital
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Aged 10-18
Diagnosis of a primary diaphyseal clavicle fracture
Fracture must be completely displaced
Patient - BCH subjects must pursue follow-up at BCH main campus or Walthammust be 59 days or less from the primary fracture
All study patients (across all sites) must agree to be contacted by a long-term follow-up coordinator based out of Boston Children's Hospital for long-term follow-up questions (out to the 2-year time point). This can/will be done via phone, mail, text message, and/or email

Exclusion Criteria

Pathological fracture
Previous ipsilateral fracture
Unable to fill out outcome collection forms
Refusal to participate
Underlying neurologic or neurocognitive disorder that affects UE function
Underlying metabolic bone disorder (e.g. osteogenesis imperfecta) that significantly alters normal bone healing
Unable to project injury X-ray films if treated initially at an institution that is not a member of this register
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