Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DEVICE | Perfecta V-Beam laser | This 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.