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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05618912
Study type Interventional
Source Indiana University
Contact
Status Completed
Phase N/A
Start date October 17, 2022
Completion date October 16, 2023

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