Vbeam Pro Pulse Dye Laser for the Treatment of Vascular Conditions

Sponsor
Candela Corporation
Study ID
NCT07290426
Status
Not Yet Recruiting

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Conditions

  • Port-Wine Stain
  • Rosacea
  • Vascular Diseases

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Vbeam Pro Laser Treatment — DEVICE
    Treatment with Vbeam Pro Laser System

Study Details

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.

Key Dates

First listed
Dec 18, 2025
Start date
Mar 31, 2026
Status verified
Dec 2025
Primary completion
Dec 31, 2028
Completion
Dec 31, 2028

Study Design

Enrollment
40 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Vbeam Pro Treatment Group
    Treatment with Vbeam Pro Laser System, up to eight (8) study treatments

Primary Outcome Measure

Clearance of Vascular Lesion [ Time Frame: Baseline to Follow-up #1 (up to 72 weeks) ]

Central Contacts

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