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Adequacy of Pain Management for Upper Extremity Fracture After Discharge From a Pediatric Emergency Depart

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01514097
Enrollment
300
Registered
2012-01-20
Start date
2012-02-29
Completion date
2016-01-31
Last updated
2015-07-30

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

Conditions

Fracture

Keywords

emergency, pediatric, fracture, pain

Brief summary

Pain is a common cause for children seeking care in the Emergency Department (ED). Children with orthopedic injuries often require pain control when seeking emergency care. Despite the high prevalence of ED visits requiring pain control, pain is often poorly assessed and treated in ED settings. Currently, no standard of care exists for the management of this fracture-related pain in children discharged from the ED. Furthermore, discrepancies in analgesia administration to patients of various racial groups seeking emergency care have been documented but are poorly understood. No research currently exists comparing pain severity between upper extremity fractures requiring simple splinting to those treated with sedated reduction and splinting. Furthermore, there is no research regarding the prevalence of significant post-discharge pain nor the differences among ethnic and age groups treated in the ED. Research Questions: What is the prevalence of significant post-discharge pain in children treated for upper extremity fractures? Is there a difference in severity between those children requiring reduction versus simple splinting? Is there a difference in pain severity noted among different ethnic or age groups? Design This is a prospective, un-blinded, observational study that will include patients seeking treatment for an upper extremity fracture.

Interventions

None listed

Sponsors

Children's Hospitals and Clinics of Minnesota
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 17 Years
Healthy volunteers
No

Inclusion criteria

* Parents/guardians of patients presenting to the ED will be included if: * The patient is younger than 18 years old * The patient has an isolated upper extremity fracture (including clavicle, humerus, forearm, wrist) undergoing ED splinting with or without reduction * The parent/guardian is English, Spanish, Somali, or Hmong-speaking * The parent/guardian lives with the child * He/she has a working telephone number

Exclusion criteria

* Potential subjects presenting to the ED will be excluded from study participation if: * There is suspicion of child abuse or neglect * The parent/guardian is not English, Spanish, Somali, or Hmong-speaking * The patient is critically ill * The fracture requires operative reduction/treatment * The patient is medically complex * The patient has a pre-existing bone disease or chronic pain syndrome

Design outcomes

Primary

MeasureTime frameDescription
Pain Scoreday 2 - 3Numeric pain scale from 0 - 10. 10 indicating the worst pain

Secondary

MeasureTime frameDescription
Second pain score assessment7-8 days after ED dischargeNumeric pain scale from 0 - 10. 10 indicating the worst pain

Countries

United States

Outcome results

None listed

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