Mederma to Reduce Appearance of Post Surgical Scars
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About
This is a single-center, 20-subject, investigator-blinded study to evaluate the effect of Mederma N&I to Mederma Ultra Gel on the appearance of post-surgical scars.
Full description
This is a 10-week research study designed to compare the effect of two gels on the appearance of post surgical scarring of the chest and/or back. The subject will be asked to identify two symmetrical skin growths that they would like to have removed: one on the left chest and/or back and one on the right chest and/or back. Additionally, the subject will identify a third skin growth that they would like removed which is a reasonable distance from the two symmetrical skin growths and will be located either on the back or the chest.
Inclusion Criteria:
- Healthy male and non pregnant female subjects ≥18 years of age
- have seborrheic keratoses on the right and left chest and/or back
Exclusion Criteria:
-Subjects with known allergies or sensitivities to ingredients contained in the test product including onion extract and Lidocaine.
Enrollment
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Inclusion criteria
- Subjects must be 18-70 years of age, of any race or sex.
- Subjects must be Fitzpatrick skin type I-VI.
- Subjects must have two symmetrical upper chest and/or back seborrheic keratoses and in the opinion of the investigator are good candidates for the study.
Exclusion criteria
- Subjects with known allergies or sensitivities to ingredients contained in the test product including onion extract and Lidocaine.
- Subjects with known history of keloids or hypertrophic scars.
Trial design
20 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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