Effect of Postoperative Dressing on Excisions Performed on the Leg: A Comparison Between Zinc Oxide Compression Dressings Versus Standard Wound Care.
Carol B Thompson, Timothy L Wiemken, Timothy S Brown
https://pubmed.ncbi.nlm.nih.gov/28654576Actively Recruiting
Led by Melissa Pugliano-Mauro · Updated on 2025-08-14
30
Participants Needed
1
Research Sites
4 weeks
Total Duration
This research investigates the healing and appearance of surgical scars on non-scalp skin closed in a straight line with a scar length of at least 4.5 cm. The study compares the effects of two ointments, zinc oxide and petrolatum, applied to different halves of each scar. This early phase 1 trial aims to evaluate scar outcomes using a validated scar assessment scale and to explore potential differences in wound healing and scar appearance between these two common skin treatments. Participants will have their surgical scars marked and divided into two halves: one side will receive zinc oxide ointment and the other petrolatum. Patients will apply the assigned ointments daily for one month while maintaining a log of their applications. Follow-up visits will occur at 1 week, 4 weeks, 8 weeks, and 6 months after surgery, during which the scars will be photographed and assessed by both the patients and trained dermatologists using the Patient and Observer Scar Assessment Scale (POSAS). The study also monitors for post-operative infections and measures the proportion of the wound that has sealed at various time points. During the study, participants will attend scheduled visits for suture removal, scar evaluation, and photographic documentation. Patients will complete questionnaires about their scar appearance at each visit. The study tracks adherence to ointment application through patient logs. Safety assessments include checking for surgical site infections and complications. Participants who complete all visits will receive a gift bag with skin care products. The total study duration per participant includes follow-up assessments up to six months post-surgery, with options for remote photo submissions if the final visit cannot be attended in person.
CONDITIONS
Zinc Oxide Versus Petrolatum Following Skin Surgery
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) for consent and enrollment at time of surgical closure
Duration - 1 month
Participants apply zinc oxide ointment to one half of their post-surgical linear scar and petrolatum ointment to the other half daily, along with daily dressing changes, for one month following surgery.
1 visit at 7 days post-op for suture removal and dressing removal; daily self-application and dressing changes at home
Duration - 6 months
Participants return for scar assessment visits where photographs are taken and scar appearance is evaluated using the POSAS scale at 4 weeks, 8 weeks, and 6 months post-operatively. Electronic photo submissions may be used if unable to attend final visit.
3 visits (in-person) at 4 weeks, 8 weeks, and 6 months post-op
Total: 1 location
1
UPMC Dermatology St. Margaret
Pittsburgh, PA, Pennsylvania, United States, 15213
Actively Recruiting
L
Lauren Crow, MD
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Carol B Thompson, Timothy L Wiemken, Timothy S Brown
https://pubmed.ncbi.nlm.nih.gov/28654576J Kantor
https://pubmed.ncbi.nlm.nih.gov/27292082