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Clinical Trials/NCT01514097
NCT01514097
Unknown
Not Applicable

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

Children's Hospitals and Clinics of Minnesota1 site in 1 country300 target enrollmentFebruary 2012
ConditionsFracture

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fracture
Sponsor
Children's Hospitals and Clinics of Minnesota
Enrollment
300
Locations
1
Primary Endpoint
Pain Score
Last Updated
10 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
January 2016
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Pain Score

Time Frame: day 2 - 3

Numeric pain scale from 0 - 10. 10 indicating the worst pain

Secondary Outcomes

  • Second pain score assessment(7-8 days after ED discharge)

Study Sites (1)

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