Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to determine whether the use of 5-0 prolene during repair of linear cutaneous surgery wounds improves scar cosmesis compared to wound closure with 5-0 fast absorbing gut (both SOC).


Clinical Trial Description

The purpose of this study is to determine whether the use of 5-0 prolene during repair of linear cutaneous surgery wounds improves scar cosmesis compared to wound closure with 5-0 fast absorbing gut (both SOC). The investigators will use a split wound model, where half of the wound is treated with 5-0 prolene and the other half is repaired with 5-0 fast absorbing gut. Three-months post-surgery, the scar will be measured via the physician observer scar assessment scale, a validated scar instrument (research procedure). The scar width and adverse events will be recorded. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02991755
Study type Interventional
Source University of California, Davis
Contact
Status Active, not recruiting
Phase N/A
Start date October 2015
Completion date September 2019

See also
  Status Clinical Trial Phase
Completed NCT02383186 - Dermal Suturing Only Versus Layered Cutaneous Closure N/A
Completed NCT02289859 - Undermining During Cutaneous Wound Closure N/A
Withdrawn NCT01352533 - Closure Techniques and Scar Appearance N/A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