Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
50 participants
INTERVENTIONAL
2025-10-23
2026-09-30
Brief Summary
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Detailed Description
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Secondary Objectives:
* Patient portion of POSAS
* Overall patient opinion of scar appearance
* Complication rate
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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A: Superior Side of the Wound
The participant's wound will be labeled A if it is on the left or superior side of the investigator
Dermabrasion
First, both sides of the wound will be sutured together with a subcutaneous (bottom) layer of stitches. Next, a predetermined, concealed randomization number will be obtained which will specify which side, A or B, will be treated with dermabrasion. An electrocautery scratch pad will be used along the wound edge of the intervention side until pin-point bleeding is achieved. This will add no additional time to the standard of care surgery time. The wound will then be closed with an epidermal (top) layer of stitches, as is the standard of care.
B: Inferior Side of the Wound
The participant's wound will be labeled B if it is on the right or inferior side of the investigator
Dermabrasion
First, both sides of the wound will be sutured together with a subcutaneous (bottom) layer of stitches. Next, a predetermined, concealed randomization number will be obtained which will specify which side, A or B, will be treated with dermabrasion. An electrocautery scratch pad will be used along the wound edge of the intervention side until pin-point bleeding is achieved. This will add no additional time to the standard of care surgery time. The wound will then be closed with an epidermal (top) layer of stitches, as is the standard of care.
Interventions
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Dermabrasion
First, both sides of the wound will be sutured together with a subcutaneous (bottom) layer of stitches. Next, a predetermined, concealed randomization number will be obtained which will specify which side, A or B, will be treated with dermabrasion. An electrocautery scratch pad will be used along the wound edge of the intervention side until pin-point bleeding is achieved. This will add no additional time to the standard of care surgery time. The wound will then be closed with an epidermal (top) layer of stitches, as is the standard of care.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Scheduled for cutaneous surgical procedure on the face or neck with predicted linear closure greater than 4 centimeters.
* Willing to return for follow up visit within the evaluation period
Exclusion Criteria
* Significant vision or hearing impairments
* Pregnant Individuals
* Incarceration
* Wounds with predicted closure length less than 4 cm
18 Years
ALL
Yes
Sponsors
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University of Wisconsin, Madison
OTHER
Responsible Party
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Principal Investigators
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Gloria Xu, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
UW School of Medicine and Public Health
Locations
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UW Health Mohs Surgery Clinic
Madison, Wisconsin, United States
Countries
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Central Contacts
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Other Identifiers
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A534300
Identifier Type: OTHER
Identifier Source: secondary_id
Protocol Version 3/21/25
Identifier Type: OTHER
Identifier Source: secondary_id
2025-0592
Identifier Type: -
Identifier Source: org_study_id