Vbeam Pro Pulse Dye Laser for the Treatment of Vascular Conditions
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCandela Corporation
About this trial
This is a clinical study to evaluate the safety and performance of the Vbeam Pro Laser System for the treatment of vascular indications, including rosacea and port wine stain birthmarks.
Eligibility criteria
Qualifiers
Healthy subjects aged 18 years or older
Presence of one or more vascular lesion, cutaneous lesion, or other dermatological condition deemed fit for treatment
Able and willing to comply with the treatment/follow-up schedule and comply with all study (protocol) requirements.
Willing to provide signed, informed consent to participate in the study
Disqualifiers
Pregnant or planning to become pregnant, having given birth less than 3 months prior to enrollment into the study, and/or breast feeding
Known photosensitivity to 595nm or 1064 nm light
History of light-induced seizure disorders
Severe unstable concurrent conditions, such as unstable cardiac disorders
Trial design
Treatments tested in this trial
- Vbeam Pro Laser Treatment
Treatment groups
40 Participants
are divided into 1 treatment groupLocations
Sponsors and collaborators
Source ClinicalTrials.gov