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Wound Eversion Versus Planar Closure for Face or Neck Wounds

Wound Eversion Versus Planar Closure for Wounds on the Face or Neck: a Randomized Split Wound Comparative Effectiveness Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03302988
Enrollment
33
Registered
2017-10-05
Start date
2015-10-13
Completion date
2017-07-25
Last updated
2018-09-24

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

Conditions

Operative Wound

Keywords

Wound Edge Eversion, Dermal Sutures

Brief summary

The aim of this study is to determine whether wound edge eversion, achieved by careful placement of dermal sutures, improves the cosmetic outcome of operative wounds closed on the head or neck.

Detailed description

It has been established that as wounds heal, the resultant tissue remodeling results in wound contracture. Surgeons are taught that by everting wounds' edges with well-placed dermal sutures, there is less depression of the resultant scar. A prior study conducted by us at this center found that wound eversion was not associated with better cosmetic outcome (1). However, it was noted that most of the procedures were performed off the head and neck, places where the effects of eversion were thought to be most beneficial (2) Thus our goal is to now study the effects of eversion exclusively on the face and neck.

Interventions

OTHEREverted closure

Suturing technique to obtain wound eversion. Type of suturing technique at surgeon's discretion

OTHERPlanar closure

The planar side will be closed with traditional buried simple closure and running cuticular sutures

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Each wound will have 2 treatments. The type of treatment (Type of suturing) will be chosen by random assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Over 18 years of age * Able to give informed consent themselves * Patient scheduled for cutaneous surgical procedure with predicted linear closure on the face or neck * Willing to return for follow up visits

Exclusion criteria

* Mentally handicapped * Unable to understand written and oral English * Incarceration * Under 18 years of age * Pregnant Women * Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers) * Pregnant women * Prisoners

Design outcomes

Primary

MeasureTime frameDescription
Patient Observer Scar Assessment Scale (POSAS)Within 3 monthsThe primary endpoint will be the score of two blinded reviewers using the physician observer assessment score at a three-month assessment visit.
Incidence of sunken scarsWithin 3 monthsThe incidence of sunken scars or elevated scaring on each treatment side will also be determined

Countries

United States

Outcome results

None listed

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