To evaluate the cosmetic outcome, effectiveness, user and subject satisfaction, and safety of LiquiBand® Flex in relation to DermaBond Advanced™ and conventional sutures for the topical closure of surgical wounds.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
66
Oncology Care Center, Beverly Hospital
Beverly, Massachusetts, United States
To compare cosmetic outcomes at follow up
Cosmesis to be evaluated by a panel of masked evaluators using a modified Hollander Wound Evaluation Scale
Time frame: 3 months post treatment
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