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CompletedNCT01938586Updated Apr 15, 2016

Comparison of Traditional Superficial Cutaneous Sutures Versus Steri-Strip Coaptive Film in Layered Dermatologic Closures

An observational study in Wound Cosmesis, sponsored by Henry Ford Health System. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-04-15.

Sponsored by Henry Ford Health System · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
10
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to compare the cosmetic outcome between buried intradermal and superficial cutaneous suture closures versus buried intradermal sutureand superficial Steri-Strip closures in the bilayered repair of dermatologic wounds on the back following elliptical excision of benign or malignant lesions

02

Conditions studied

  • Wound Cosmesis

Keywords

  • Scar
  • Appearance
03

In context

Lead sponsor

Henry Ford Health System is the lead sponsor of 293 studies on the registry; 50 are open to participants now.

Of its 35 completed or terminated interventional studies of FDA-regulated products, 23 (66%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Outpatient dermatology clinic

Inclusion criteria

  • 18 years or greater in age
  • Simple excision of benign or malignant lesion on the back
  • Final scar length of at least 3cm

Exclusion criteria

Exclusion Criteria:

  • Known history of keloid formation or hypertrophic scars
  • Known adhesive allergy
  • Pregnancy or active breast feeding
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
10 participants (actual)
Patient registry
No

Groups and cohorts

  • Surgical excision

    Other: Steri-Strip · Other: Superficial sutures

Interventions

  • OtherSteri-Strip
  • OtherSuperficial sutures
06

What researchers measure

Primary outcomes

  1. Overall scar appearance as evaluated by the Patient and Observer Scar Assessment Scale

    Time frame: 6 months

Secondary outcomes

  1. Rates of postoperative complications

    Assessment of scar erythema, swelling, infection, drainage, dehiscence

    Time frame: 6 months

  2. Time for closure of each split half portion of wound

    Time frame: 1 hour (intraoperative)

07

Study locations

1 site
  • Henry Ford Dermatology Clinic
    Detroit, Michigan 48202, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 15, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01938586
Lead sponsor
Henry Ford Health System
Responsible party
David M. Ozog (Director of Cosmetic Dermatology, Vice-Chair of Operations, Henry Ford Health System) — Principal investigator
First posted
Sep 10, 2013
Start date
Nov 2013
Primary completion
Jun 2014
Completion
Aug 2014
Last update
Apr 15, 2016
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2013. You cannot join it, but the record below documents what was studied.

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