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NCT05618912 · ClinicalTrials.gov registry record · NA
Scar Appearance After Postoperative Hydrocolloid Dressing Versus Standard Petrolatum Ointment
A NA study, sponsored by Indiana University.
- Completed
- Registry status
- NA
- Development phase
- 146
- Enrollment target
NCT05618912 is a NA study that has completed, run by Indiana University. The registered enrollment target is 146 participants.
The verdict
NCT05618912, a NA study, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- NA
- Development phase
- 146 participants
- Enrollment target
Study 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.
Interventions
- DEVICE Hydrocolloid dressing
- OTHER Petrolatum jelly dressing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 146 participants |
| Start Date | 2022-10-17 |
| Est. Completion | 2023-10-16 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05618912
The ClinicalTrials.gov registry entry for NCT05618912 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 146 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Hydrocolloid dressing is the first listed.
NCT05618912 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05618912 about?
NCT05618912 is a clinical study titled "Scar Appearance After Postoperative Hydrocolloid Dressing Versus Standard Petrolatum Ointment". 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 ...
What is the current status of trial NCT05618912?
This trial is currently completed. It is a NA study. The enrollment target is 146 participants. The study started on 2022-10-17. Estimated completion is 2023-10-16.
What interventions are being tested in trial NCT05618912?
The interventions under investigation include: Hydrocolloid dressing (DEVICE), Petrolatum jelly dressing (OTHER).
Who is sponsoring clinical trial NCT05618912?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
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