Actively Recruiting

Early Phase 1
Age: 18Years +
All Genders
Healthy Volunteers
ID03561376

Zinc Oxide Versus Petrolatum Following Skin Surgery: A Head-to-head, Prospective, Split-scar Study

Led by Melissa Pugliano-Mauro · Updated on 2025-08-14

30

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Zinc Oxide Versus Petrolatum Following Skin Surgery

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Linear closure on non-scalp skin
  • Scar length of 4.5 cm or greater
  • Scar is symmetrical from end to end
  • Surgical site is not infected
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Visibly asymmetrical linear scar
  • Grossly infected surgical site
  • Known allergy to topical zinc oxide

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

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

Treatment

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

Follow-up

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

Trial Site Locations

Total: 1 location

1

UPMC Dermatology St. Margaret

Pittsburgh, PA, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

L

Lauren Crow, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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Published Research Related To This Trial

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/28654576