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Feasibility Study to Collect and Assess Safety Data for a Radiofrequency Microneedling Device for Electrocoagulation and Hemostasis of Soft Tissues for Dermatologic Conditions

Wrinkle Clinical Trial

Official title:
Feasibility Study to Collect and Assess Safety Data for a Radiofrequency Microneedling Device for Electrocoagulation and Hemostasis of Soft Tissues for Dermatologic Conditions.

Clinical Trial Summary

The goal of the Potenza device used in this study is to collect clinical data for dermatologic conditions in which electrocoagulation and hemostasis is a viable mechanism for means of improvement.

Clinical Trial Description

Up to 12 subjects will be enrolled at 1 study center. Subjects will be enrolled into 2 groups. Group A will receive treatments on the face, neck, and/or body. Group B will receive split-face treatments where each side of the face may be treated with different tips. Subjects will attend a screening/pretreatment visit which may be performed on the same day as the treatment visit. Subjects may receive up to 5 treatments. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05987319
Study type Interventional
Source Cynosure, Inc.
Contact Jamie Trimper
Phone 9782564200
Email jamie.trimper@cynosure.com
Status Recruiting
Phase N/A
Start date July 24, 2023
Completion date August 2024
View Details
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