Know Cancer

or
forgot password

Combined Photodynamic and Pulsed Dye Laser Treatment of Port Wine Stains


N/A
18 Years
N/A
Open (Enrolling by invite only)
Both
Port Wine Stains

Thank you

Trial Information

Combined Photodynamic and Pulsed Dye Laser Treatment of Port Wine Stains


Procedures will be performed at the Surgery Laser Clinic at the Beckman Laser Institute at
the University of California, Irvine.

At an initial visit, a brief history and physical will be performed.

The history will include: 1) previous treatment to my PWS; 2) current medications; 3)
history of light sensitivity; 4) risk of pregnancy and use of birth control in a female of
child-bearing age.

The physical will include: 1) measurement and evaluation of PWS; 2) measurement of blood
pressure, blood cell count, general chemistries (including liver function tests) and ANA,
which might indicate an increased sensitivity to light.

On the day of treatment, the same brief physical and history will be repeated. A urine
pregnancy test will be performed on females of child-bearing age.

Four circular test sites of PWS will be selected. One test site will receive no treatment.
The second test sites will be treated with the pulsed dye laser at standard setting and
protective eyeglasses to shield the eyes during the laser treatment.

For two additional test spots, the photodynamic therapy (PDT) verteporfin will be
administered intravenously over a 10-minute period. After receiving the verteporfin, the
skin and eyes will be sensitive to light for the next 5 days. The light sensitive protection
precautions will be instructed.

Optical Doppler Tomography unit (ODT) measurements, similar to shining a flash light to PWS
and measuring the light response, which provide information about how blood is flowing
through the PWS.

Photographs and light measurements will be taken during follow-up visits on day 1, day 3,
and 1, 2, 4, 8 and 12 weeks after the study treatment. At these visits blood may also be
drawn to check for blood substances that promote blood vessel formation.

At the end of the study, blood tests will be drawn to assess cell count and general
chemistries.


Inclusion Criteria:



- Adult 18 years and older

- Have a PWS on an area other than the face

- A negative pregnancy test and non pregnant or nursing

Exclusion Criteria:

- Under 18 years of age

- Have an allergy to verteporfin, porfimer sodium or other porphyrins

- Have a history of porphyria (a disease that can cause sensitivity to light)

- Have had treatment to the PWS test sites in the last 8 weeks

- Have an active uncontrolled infection or other significant disease

- Currently using medications that cause sensitivity to light such as tetracyclines,
sulfonamides, phenothiazines, sulfonylurea hypoglycemic agents, thiazide diuretics
and griseofulvin

- Currently using medications that increase bleeding, including aspirin, coumadin or
non-steroidal anti-inflammatory drugs

- Have very dark skin which is sensitive to laser treatment

- Have a positive ANA (lab tests which indicates sensitivity to light)

Type of Study:

Interventional

Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Combined sub-threshold photodynamic and pulsed dye laser therapy can be used to safely achieve improved PWS lesion lightening as compared to either sub-threshold photodynamic therapy or pulsed dye laser therapy alone

Outcome Time Frame:

12 weeks

Safety Issue:

Yes

Principal Investigator

Kristen Kelly, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Beckman Laser Institute University of California Irvine

Authority:

United States: Institutional Review Board

Study ID:

ASLMS-47456

NCT ID:

NCT00556946

Start Date:

August 2005

Completion Date:

July 2015

Related Keywords:

  • Port Wine Stains
  • Vascular Malformation
  • Port-Wine Stain

Name

Location

Beckman Laser Medical Clinic,University Irvine, California  02612