Clinical Trials Directory

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UnknownNCT03211585

EVALUATION OF THE EFFECT OF THE PERFECTA V-BEAM LASER ON ROSACEA

EVALUATION OF THE EFFECT OF THE PERFECTA V-BEAM LASER ON ROSACEA (FACIAL REDNESS, TELANGIECTASIAS AND PHOTODAMAGE)

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Syneron Medical · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to further quantify the safety and effectiveness of the Syneron-Candela long pulse-duration, extended sub-pulse, larger spot-size prototype Perfecta V-Beam, 595nm laser system for the treatment of facial redness associated with flushing and blushing, or rosacea. The Perfecta laser system is expected to provide effective treatment of rosacea with less bruising or purpura and greater effectiveness than previous generation systems. This study should enable optimization of treatment parameters for using the Perfecta 595nm laser for treating rosacea.

Conditions

Interventions

TypeNameDescription
DEVICEPerfecta V-Beam laserThis s a single study and a prototype of the FDA-cleared, flashlamp-pumped pulsed-dye laser, that is currently on the market, that has evolved over almost 25 years of continuous development. The broad-spectrum flashlamp pumps energy into a cavity containing liquid dye. The dye is excited resulting in the emission of 595 nm orange light.

Timeline

Start date
2016-10-01
Primary completion
2018-04-01
Completion
2018-12-01
First posted
2017-07-07
Last updated
2017-07-12

Source: ClinicalTrials.gov record NCT03211585. Inclusion in this directory is not an endorsement.