Status:
COMPLETED
An Analysis of Dermabond vs. Non-Absorbable Sutures in Skin Closure for Brow Ptosis Procedures
Lead Sponsor:
Cody Blanchard
Conditions:
Brow Ptosis
Surgical Wound
Eligibility:
All Genders
18-100 years
Phase:
NA
Brief 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 equiva...
Eligibility Criteria
Inclusion
- Patients undergoing bilateral direct excision brow lift for brow ptosis at the University of Kentucky Medical Center.
- Patients \> 18 years of age.
- Patients must be able to follow up at the specified intervals.
- Patients who are able to give their own informed consent.
- Health Status: Variable health status reflective of general population of Kentucky. Patients will be healthy enough to be seen in an office setting.
- All patients will need to be proficient in the English language to understand the scale used for scar assessment
Exclusion
- Patients \<18 years of age or \>100
- Allergy to Dermabond
- Adults with impaired consent capacity
- Incarcerated individuals
Key Trial Info
Start Date :
August 15 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 17 2024
Estimated Enrollment :
8 Patients enrolled
Trial Details
Trial ID
NCT05981443
Start Date
August 15 2023
End Date
April 17 2024
Last Update
April 24 2025
Active Locations (1)
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1
University of Kentucky
Lexington, Kentucky, United States, 40508