Trials / Completed
CompletedNCT01504061
Mederma to Reduce Appearance of Post Surgical Scars
The Comparison of Mederma® N&I to Mederma® Ultra Gel to Reduce the Appearance of Post Surgical Scars
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Merz North America, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
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.
Detailed 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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Mederma N&I | Topical gel applied three times a day for eight weeks. |
| OTHER | Mederma Ultra Gel | Topical gel applied once daily for eight weeks. |
Timeline
- Start date
- 2012-01-01
- Primary completion
- 2012-06-01
- Completion
- 2012-08-01
- First posted
- 2012-01-05
- Last updated
- 2013-10-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01504061. Inclusion in this directory is not an endorsement.