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Cosmetic Outcomes and Patient Satisfaction After Facial Laceration Repair in the Emergency Department

C

Children's Hospitals and Clinics of Minnesota

Status

Completed

Conditions

Facial Lacerations

Study type

Observational

Funder types

Other

Identifiers

NCT01514084
1108-081

Details and patient eligibility

About

Facial lacerations are commonly treated in the emergency department. The nature of the injury leads to a great deal of concern about the long-term cosmetic appearance of the wounds.

Research Questions

  1. What is the association between wound characteristics, wound management in the ED, patient satisfaction in the ED, and patient-rated cosmetic appearance of sutured wounds?
  2. Is there a difference noted among ED providers with different levels of training?
  3. Is there an association between initial satisfaction scores and wound outcome?
  4. Is there an association between short term and long term wound scores?

Design This is a non-randomized, prospective, observational study of patients who present to the ED seeking treatment for facial laceration repair.

Enrollment

160 estimated patients

Sex

All

Ages

Under 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Families presenting to the ED for repair of facial laceration will be approached for study inclusion if:

    • Their child seeking treatment is less than 18 years of age
    • The laceration was sustained less than 12 hours prior to presentation to Children's ED
    • They speak English

Exclusion criteria

  • Families presenting to the ED for repair of facial laceration will be excluded from study participation if they:

    • Are medically complex children
    • Have a history of pre-existing coagulopathy or collagen vascular disease
    • Have a history of immunodeficiency or diabetes mellitus
    • Are suspected of non-accidental trauma
    • Have wounds that could be approximated by tissue adhesives
    • Have animal or human bites
    • Have gross contamination
    • Have puncture wounds
    • Have lacerations of tendon/nerve/cartilage
    • Have scalp lacerations
    • Do not speak English

Trial design

160 participants in 4 patient groups

PEM group
Description:
Patients whose lacerations have been repaired by PEM trained physicians.
GP group
Description:
Patients whose lacerations have been repaired by general pediatricians.
PNP group
Description:
Patients whose lacerations have been repaired by PNPs.
RN group
Description:
Patients whose lacerations have been repaired by suture RNs.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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