Trials / Completed
CompletedNCT05618912
Scar Appearance After Postoperative Hydrocolloid Dressing Versus Standard Petrolatum Ointment
Scar Appearance After Postoperative Hydrocolloid Dressing Versus Standard Petrolatum Ointment: A Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 146 (actual)
- Sponsor
- Indiana University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
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.
Conditions
- Scar
- Skin Scarring
- Skin Cancer
- Wound Heal
- Wound of Skin
- Surgical Wound
- Patient Satisfaction
- Patient Preference
- Surgical Incision
Interventions
| Type | Name | Description |
|---|---|---|
| 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. |
Timeline
- Start date
- 2022-10-17
- Primary completion
- 2023-10-16
- Completion
- 2023-10-16
- First posted
- 2022-11-16
- Last updated
- 2024-12-11
- Results posted
- 2024-12-11
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05618912. Inclusion in this directory is not an endorsement.