Dermal Cryotherapy in Patients Undergoing Abdominoplasty

Status Completed

Clinical Trial Summary

A prospective, interventional, single-arm study to evaluate histologic changes in skin following cryotherapy with the study device.

Clinical Trial Description

This study is to include healthy adults who intend to undergo an abdominoplasty surgery, and agree to have small areas of their middle and lower abdomen exposed to cooling with the Dermal Cooling System within 180 days before the planned surgery. Exposure of multiple test sites will be completed in areas of skin that will be excised as part of the abdominoplasty procedure. Clinical assessments of the treatment sites at 1-week post-treatment and at 1-month post-treatment intervals throughout the time period prior to surgical excision, and histologic evaluation of the treated skin will be conducted to assess skin changes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02763306
Study type	Interventional
Source	R2 Dermatology
Contact
Status	Completed
Phase	N/A
Start date	June 2015
Completion date	April 2017

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