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Laser Therapy Versus Electrosurgery For Nasal Telangiectasias

Not Applicable
Withdrawn
Conditions
Telangiectasis
Interventions
Device: Long Pulsed Alexandrite Laser
Device: Pulsed Dye Laser
Procedure: Electrodesiccation
Registration Number
NCT02090517
Lead Sponsor
University of California, Davis
Brief Summary

The aim of this study is to compare the efficacy of various treatment options for eliminating nasal telangiectasias. The study will compare the outcome of treating nasal telangiectasias with the following; no treatment (control site), alexandrite laser, pulsed dye laser, combination pulsed dye laser and Nd:YAG 1064nm multiplex laser system and electrosurgery.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Over 18 years of age
  • Able to give informed consent themselves
  • Willing to return for follow up visit
  • 0.5 - 3 millimeter Vessel size
  • 5 Non-contiguous nasal vascular lesions
Exclusion Criteria
  • Mentally handicapped
  • Unable to understand written and oral English
  • Incarceration
  • Under 18 years of age
  • Unwilling to return for follow up
  • Pregnant Women
  • Vessels less than 0.5 millimeter caliber
  • Less than 5 non-contiguous vessels

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Long Pulsed Alexandrite LaserLong Pulsed Alexandrite LaserSubjects with multiple nose telangiectasias will be enrolled. One nose telangiectasia (of 5) will be treated with long pulsed alexandrite laser.
Pulsed Dye LaserPulsed Dye LaserSubjects with multiple nose telangiectasias will be enrolled. One nose telangiectasia (of 5) will be treated with pulsed dye laser.
ElectrodesiccationElectrodesiccationSubjects with multiple nose telangiectasias will be enrolled. One nose telangiectasia (of 5) will be treated with electrodesiccation.
Primary Outcome Measures
NameTimeMethod
Reduction of Area of Nasal Telangiectasias by Laser Therapy Vs Electrosurgery3 months

The study will measure the changes in length and width (area) of nasal telangiectasias before and after treatment with the following: no treatment (control site), alexandrite laser, pulsed dye laser, combination pulsed dye laser and Nd:YAG 1064nm multiplex laser system and electrosurgery.

Secondary Outcome Measures
NameTimeMethod
Evaluation of Cosmetic Improvement3 months

Percent perceived improvement for nasal vessels by the patient via questionnaire.

Trial Locations

Locations (1)

University of California-Davis, Department of Dermatology

🇺🇸

Sacramento, California, United States

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