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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05618912
Other study ID # 15768
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 17, 2022
Est. completion date October 16, 2023

Study information

Verified date June 2024
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

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.


Recruitment information / eligibility

Status Completed
Enrollment 159
Est. completion date October 16, 2023
Est. primary completion date October 16, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Device:
Hydrocolloid dressing
A single hydrocolloid dressing will be applied to the surgical site for 7 days following dermatologic surgery
Other:
Petrolatum jelly dressing
The patient with the control wound will be covered with petrolatum jelly during this time period, which has to be re-applied daily.

Locations

Country Name City State
United States IU Health Physicians Dermatology Meridian Crossing Carmel Indiana

Sponsors (1)

Lead Sponsor Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Holmes SP, Rivera S, Hooper PB, Slaven JE, Que SKT. Hydrocolloid dressing versus conventional wound care after dermatologic surgery. JAAD Int. 2021 Dec 21;6:37-42. doi: 10.1016/j.jdin.2021.11.002. eCollection 2022 Mar. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Cosmetic outcome Patient and surgeon assessment of cosmetic outcome using modified visual analogue scar scale. The minimum value is 1 and the maximum value is 10. 1 is the worst possible scar appearance and 10, is the best possible scar appearance. 7 days
Primary Cosmetic outcome Patient and surgeon assessment of cosmetic outcome using modified visual analogue scar scale. The minimum value is 1 and the maximum value is 10. 1 is the worst possible scar appearance and 10, is the best possible scar appearance. 30 days
Primary Cosmetic outcome Patient and surgeon assessment of cosmetic outcome using modified visual analogue scar scale. The minimum value is 1 and the maximum value is 10. 1 is the worst possible scar appearance and 10, is the best possible scar appearance. 90 days
Secondary Complication rate Complication rate including hematoma, seroma, wound infection requiring antibiotics, opening and drainage of wound, dehiscence. Complications will be assessed by physicians other than operating surgeon 7 days, 30 days, 90 days
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