Clinical Trials Logo

Clinical Trial Summary

Port wine stain are a congenital, progressive vascular malformation of human skin. The pulsed dye laser is approved by the Food and Drug Administration for the treatment of choice. However, the degree of port wine stain blanching seen following pulsed dye laser treatment remains variable and unpredictable. If the ultimate standard required is complete lesion blanching, the average success rate is below 10%, even after undergoing numerous pulsed dye laser treatments. Moreover, less than 50% of patients achieve 50% fading of their Port wine stain in response to pulsed dye laser therapy.


Clinical Trial Description

The researchers' specific aim is to determine whether the use of the pulsed dye laser operating at a wavelength of 577 nm will improve therapeutic outcome as compared to a pulsed dye laser operating at 595 nm. The researcher can treat port wine stain treated using a pulsed dye laser operating at a wavelength of 577 nm and the other half at a wavelength of 595 nm. The researcher can determine that the 577 nm pulsed dye laser improved port wine stain blanching responses more than the areas treated with 595 nm. The degree of port wine stain blanching which will determine by visible reflectance spectroscopy skin imaging device measurements. Post-treatment blanching responses can compare with pre-treatment measurements of port wine stain fractional blood volume. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00573729
Study type Interventional
Source University of California, Irvine
Contact
Status Completed
Phase Phase 1
Start date March 2007
Completion date January 2009

See also
  Status Clinical Trial Phase
Terminated NCT00979550 - The Effects of Aldara as an Adjunct to Laser Treatment Phase 2
Completed NCT01101360 - Port Wine Stains Treatment Matrix RF Study N/A
Completed NCT00556946 - Combined Photodynamic and Pulsed Dye Laser Treatment of Port Wine Stains N/A