University of Kentucky
Lexington, Kentucky, 40508, United States
NCT Number: NCT07075159
This study aims to explore the use of a hydrocolloid dressing (DuoDERM EXTRA THIN) as an alternative to the current standard of care. The dressing would be applied immediately after surgery and removed at a post-operative week 1 appointment. The dressing would eliminate the need for antibiotic ointment application and reduce the burden of post-operative care on the patient.
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Notify Me18 year–100 year
All sexes
Interventional
Not applicable
Lexington, Kentucky, 40508, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
one time hydrocolloid dressing application
Other names: DuoDERM Extra Thin dressing
Time frame: 3 months
YES/NO type question if wound dehiscence is present after removal of the patch
Time frame: 3 months
Patient and Observer Scar Assessment Scale filled out by both patient and provider at postoperative visit of both HCD Dressing and ointment. This survey is scaled from 0-10, with 0 being normal skin and 10 being very different skin. Lower scores are desired on this survey.
Janice Hernandez, MD
Other
Acronym: HCD Wound Heal
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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