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Clinical Trial Summary

The goal of this clinical trial is to compare Dermabond with non-absorbable sutures in skin closure after brow ptosis surgery. The main questions it aims to answer are: - if Dermabond provides equivalent wound healing compared to conventional non-absorbable skin suture techniques - if Dermabond provides equivalent scar appearance compared to conventional non-absorbable suture techniques - if Dermabond results in equivalent complication rates compared to conventional non-absorbable suture techniques Participants will have be randomly selected to have either Dermabond or non-absorbable suture closure methods. Scar analysis and both participant and provider surveys will be performed to assess the differences between groups, if any.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05981443
Study type Interventional
Source University of Kentucky
Contact Cody Blanchard, MD
Phone 859-323-5875
Email cody.blanchard@uky.edu
Status Recruiting
Phase N/A
Start date August 15, 2023
Completion date June 2024

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