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Port Wine Stains Treatment Matrix RF Study

NCT01101360 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2014-12-02

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and safety of the Matrix RF for Port Wine Stains based on clinical and histological analyses.

Conditions

  • Port Wine Stains

Interventions

DEVICE

Matrix RF

Section of port wine stain to be treated 5 times every 5 weeks (+/- 1 week)

DEVICE

Matrix RF followed by Pulse Dye Laser

Section of port wine stain to be treated 5 times every 5 weeks (+/- 1 week)

DEVICE

Pulse Dye Laser followed by Matrix RF

Section of port wine stain to be treated 5 times every 5 weeks (+/- 1 week)

Sponsors & Collaborators

  • Syneron Medical

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2011-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01101360 on ClinicalTrials.gov