Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care

Outcome Measure:

Everted versus non-everted suturing techniques

Outcome Description:

Primary outcome measures for this study are the post operative scar width measured at 1 cm from the midline on both sides of the scar.

Outcome Time Frame:

3 and 6 months

Safety Issue:

No

Principal Investigator

Daniel Eisen, M.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

University of California, Davis

Authority:

United States: Institutional Review Board

Study ID:

265161

NCT ID:

NCT01770002

Start Date:

January 2012

Completion Date:

November 2013

Related Keywords:

• Basal Cell Carcinoma
• Squamous Cell Carcinoma
• Melanoma
• Carcinoma
• Carcinoma, Basal Cell
• Carcinoma, Squamous Cell
• Melanoma