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Rate of Allergic Contact Dermatitis and Cosmetic Outcomes for Three Wound Closure Techniques in Joint Arthroplasty Patients: A Randomized, Controlled Trial
The patients from the Department of Orthopaedics Center for Joint Replacement will be asked to participate in the study. These patients will be randomized to one of three wound closure products, Sylke adhesive dressing, Exofin skin glue, or Suture Strip Plus. Participants will be asked to take a photograph of the incision 4 days after surgery to submit via MyChart for review by the WVU Department of Dermatology Team. All patients will be evaluated at their regular 2-week, 6-week, and 3-month post-operative visits where clinical photographs will be submitted for independent review by the WVU Department of Dermatology Team to assess outcomes.
Age
18 - 80 years
Sex
ALL
Healthy Volunteers
No
West Virginia University
Morgantown, West Virginia, United States
Start Date
July 21, 2025
Primary Completion Date
February 1, 2028
Completion Date
June 1, 2028
Last Updated
July 28, 2025
600
ESTIMATED participants
Sylke Adhesive Dressing
PROCEDURE
Exofin Skin Glue
PROCEDURE
Suture Strip Plus
PROCEDURE
Lead Sponsor
West Virginia University
NCT07364578
NCT06488144
NCT07058623
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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