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The Effect of Wound Edge Eversion on Cosmesis

The Effect of Wound Edge Eversion on Cosmesis

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00872638
Enrollment
0
Registered
2009-03-31
Start date
2008-01-31
Completion date
2016-04-30
Last updated
2015-06-01

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

Conditions

Surgical Incisions

Keywords

wound edge eversion, cosmetic outcomes, surgical incisions

Brief summary

Aesthetic appearance of repaired incisions is very important to surgical patients. It has been stated that if the edges of a wound are closed in such a manner that will result in eversion, or pouting of the edges that the end cosmetic result will be superior when compared to wound edges that are simply approximated. The purpose of this study is to compare cosmetic outcomes of incisions that are closed with everted edges to those in which the edges are simply approximated.

Detailed description

Surgical incisions will be split into two halfs and each half will be randomized to standard or everting sutures. 3 months later the cosmetic outcome of the healed wounds will be determined using a validated scar evaluation scale.

Interventions

PROCEDUREEversion

Surgical incisions will be closed in such a manner so as to evert the wound edges.

PROCEDUREApproximation

Surgical incisions will be closed in such a manner so that wound edges are approximated exactly, i.e. without eversion.

Sponsors

Stony Brook University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

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

Inclusion criteria

* age over 18. * able to consent. * scheduled for elective plastic or cardiothoracic surgery.

Exclusion criteria

* history of keloids, hypertrophic scarring, diabetes, or peripheral vascular disease. * those requiring systemic steroids or undergoing chemotherapy, and those unable or unwilling to consent.

Design outcomes

Primary

MeasureTime frame
Cosmetic result of surgical incision as measured by VAS scale1 year

Secondary

MeasureTime frame
Cosmetic Results as measured by the Stony Brook Scar Scale1 year

Countries

United States

Outcome results

None listed

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