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Scar Appearance After Postoperative Hydrocolloid Dressing Versus Standard Petrolatum Ointment

Indiana University logo

Indiana University

Status

Completed

Conditions

Patient Preference
Surgical Wound
Skin Scarring
Patient Satisfaction
Wound of Skin
Surgical Incision
Skin Cancer
Wound Heal
Scar

Treatments

Device: Hydrocolloid dressing
Other: Petrolatum jelly dressing

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Patients will be randomized either to receive standard daily dressing or hydrocolloid dressing using a randomization generator. After closing the wound with the sutures,the scar will be covered by a hydrocolloid dressing, which will be left in place for 7 days(Experimental) or the standard dressing (Control) that will be covered with petrolatum jelly and bandaging during this time period, which has to be re-applied daily. Patients and dermatologic surgeons will then complete surveys 7 days, 30 days, and 90 days after surgery to evaluate the cosmetic appearance of these scars.

Enrollment

146 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Adult > 18 years of age
  2. Linear scars
  3. Patients underwent conventional excision or Mohs micrographic surgery for primary cutaneous cancer or other cutaneous condition that required surgical intervention

Exclusion criteria

  1. Scar localization on acral or hair bearing sites
  2. Patients unable to converse in English
  3. Patients requiring flap or graft for closure of wound
  4. History of allergy to adhesives
  5. Patient using topical chemotherapy agents on the surgical site or planning to start it within 3 months after surgery
  6. Use of hydrocolloid dressings for post-operative wound care in the past

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

146 participants in 2 patient groups

hydrocolloid dressing arm
Experimental group
Description:
After informed consent and closing the wound with the sutures, the scar will be covered by a hydrocolloid dressing, which will be left in place for 7 days (Experimental)
Treatment:
Device: Hydrocolloid dressing
Petrolatum jelly dressing arm
Active Comparator group
Description:
and the other group of patients (control), after closing the wound with the sutures, the scar will be covered with petrolatum jelly during this time period, which has to be re-applied daily.
Treatment:
Other: Petrolatum jelly dressing

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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