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Clinical Trial Summary

The goal of this study is to assess whether wound closure with skin adhesive or running stitches combined with skin adhesive will be superior to standard wound sutures. This is a split-wound study that will compare two methods of skin closure within one standard closure technique, thereby providing an internal control of running stitches within each wound. The investigators plan to measure outcomes by assessing for scar appearance, the incidence of wound opening, scar elasticity and subject satisfaction.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01352533
Study type Interventional
Source Northwestern University
Contact
Status Withdrawn
Phase N/A
Start date July 2016
Completion date July 2017

See also
  Status Clinical Trial Phase
Active, not recruiting NCT02991755 - Use of 5-0 Prolene Versus 5-0 Fast Absorbing Gut During Cutaneous Wound Closure N/A
Completed NCT02383186 - Dermal Suturing Only Versus Layered Cutaneous Closure N/A
Completed NCT02289859 - Undermining During Cutaneous Wound Closure N/A
Completed NCT02547077 - Use of 2-octylcyanoacrylate (Dermabond) Versus 5-0 Fast Absorbing Gut During Cutaneous Wound Closure N/A
Completed NCT02550574 - Use of 2-octylcyanoacrylate With Full-thickness Skin Grafts N/A
Completed NCT02062866 - Evaluation of Purse-String Closure Vs Second Intention N/A