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Comparing Pressure Versus Simple Adhesive Dressing After Mohs Reconstruction

Comparing Pressure Versus Simple Adhesive Dressing After Mohs Reconstruction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02780934
Enrollment
81
Registered
2016-05-24
Start date
2015-10-31
Completion date
2016-05-31
Last updated
2016-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-melanoma Skin Cancer

Keywords

Pressure Dressing, Post-operative Care, Simple Adhesive Dressing, Mohs

Brief summary

The purpose of this study is to determine whether using a pressure- vs. simple adhesive dressing affects the postoperative course and wound healing outcomes following Mohs surgery.

Detailed description

The investigators will randomize patients undergoing Mohs surgery to receive either a pressure or a simple adhesive dressing following their procedure. The hypothesis is that patients with the simple adhesive dressings will be more satisfied and comfortable with their wound care on follow-up. These patients are also expected to cite greater convenience managing the simple dressing at home. Finally, the investigators anticipate no difference in the number of postoperative complications between the two groups and expect that there will be a lower cost associated with the simple adhesive dressing as compared to the pressure dressing.

Interventions

Patients in this group will receive the standard post-operative bandage: a pressure dressing consisting of high absorbency gauze and retention tape.

OTHERSimple Adhesive Dressing

Patients in this group will receive the experimental bandage: a simple adhesive dressing consisting of a non adherent pad and transparent dressing.

Sponsors

Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients will be considered for enrollment if they have been referred to a Mohs surgeon for consideration of Mohs surgery for non-melanoma skin cancer.

Exclusion criteria

* Lack of indication for Mohs * Significant comorbidities * Case of a high-risk location or tumor size which necessitates consultation with other specialties in advance.

Design outcomes

Primary

MeasureTime frameDescription
Patient SatisfactionAssessed at the first clinical follow-up visit, 1-2 weeks following Mohs procedurePatients are asked to complete a survey regarding their satisfaction with their post-operative dressing. Surveys will be distributed at their first clinical follow-up visit. They are asked to rate their overall satisfaction and difficulty sleeping, bathing, and returning to normal activity following their Mohs procedure.
ComplicationsAssessed at the first clinical follow-up visit, 1-2 weeks following Mohs procedureThe number of complications requiring medical attention in each arm of the study. These complications include: infection, bleeding, wound dehiscence, splitting or retained stitches, pain, and cosmetic disfigurement.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026