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Laser Therapy

Excel V 532 nm KTP Laser for Treatment of Erythematotelangiectatic Rosacea & Papulopustular Rosacea

N/A
Waitlist Available
Led By Stephen Ronan, MD
Research Sponsored by Cutera Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 0, 4 weeks, 8 weeks, 16 weeks
Awards & highlights
No Placebo-Only Group

Summary

A single center prospective, randomized, controlled split face study comparing a 532nm KTP laser with a 595nm PDL for the treatment of Erythematotelangiectatic Rosacea and Papulopustular Rosacea. Subjects will receive laser treatments and will be followed at 6 weeks post-final laser treatment.

Eligible Conditions
  • Rosacea
  • Papulopustular Rosacea

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 0, 4 weeks, 8 weeks, 16 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and day 0, 4 weeks, 8 weeks, 16 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Degree of Improvement in Erythematotelangiectatic Rosacea and Papulopustular Rosacea
Secondary study objectives
Adverse Events
Change in Dermatology Life Quality Index
Comparison of improvement in Erythematotelangiectatic Rosacea and Papulopustular Rosacea between the treatment arms prior to the 2nd and 3rd treatment, and at 4-6 weeks post-final treatment as assessed using Subject's Comparative Face Assessment Scale.
+5 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: 532nm KTP Laser vs 595nm Pulse Dye LaserExperimental Treatment1 Intervention
This is a single-center prospective, randomized, controlled split-face study in 20 subjects diagnosed with Erythematotelangiectatic Rosacea and/or Papulopustular Rosacea. This two arm, split-face study will consist of: 1. Treatment arm involving treatments with 532nm KTP laser 2. Active control arm involving treatments with 595nm Pulse Dye Laser (PDL) Each subject's face will be divided in half and labeled as A (Right Side of the Face) or B (Left Side of Face). The allocation of treatment (532nm KTP laser) and active control treatment (595nm PDL) arms will be determined by randomization.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
532nm KTP Laser vs 595nm Pulse Dye Laser
2014
N/A
~30

Find a Location

Who is running the clinical trial?

Cutera Inc.Lead Sponsor
43 Previous Clinical Trials
1,164 Total Patients Enrolled
1 Trials studying Rosacea
20 Patients Enrolled for Rosacea
Stephen Ronan, MDPrincipal InvestigatorStudy Principal Investigator
9 Previous Clinical Trials
219 Total Patients Enrolled
1 Trials studying Rosacea
20 Patients Enrolled for Rosacea
~2 spots leftby Jan 2026