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Functional Usability and Feasibility Testing of the Profound Matrix™ System

Wrinkle Clinical Trial

Official title:
Functional Usability and Feasibility Testing of the Profound Matrix™ System

Clinical Trial Summary

This is a non-randomized, multi-center, open-label clinical trial evaluating the efficacy and clinical feasibility of the Profound Matrix device for electrocoagulation and for treatment of wrinkles and acne scars. Subjects will receive up to three (3) treatments with the Matrix Pro applicator or up to five (5) treatments with the Sublime and/or Sublative Radiofrequency (RF) applicators.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06192550
Study type Interventional
Source Candela Corporation
Contact
Status Active, not recruiting
Phase N/A
Start date October 28, 2020
Completion date July 2024
View Details
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