Treatment of Naevus Flammeus Using Intense Pulsed Light and Pulsed Dye Laser
Not Applicable
Completed
- Conditions
- Port-Wine Stain
- Registration Number
- NCT00365118
- Lead Sponsor
- Bispebjerg Hospital
- Brief Summary
The purpose of the trial is to compare efficacy and adverse effects of pulsed dye laser and intense pulsed light in patients with port wine stains.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Patients with previously untreated and previously laser-treated naevus flammeus. Naevus flammeus measuring at least 5 x 7 cm within a single anatomical area. For example, the face corresponding to dermatomes V1, V2 and V3, back, abdomen, arms and legs.Patients aged two or above.Patients with skin types I-III.
Exclusion Criteria
- Patients below two years of age.
- Pregnant or breastfeeding patients.
- Patients with known increased sensitivity to visible light.
- Patients with a tendency to produce hypertrophic scars or celoids.
- Patients with skin types IV, V and VI.
- Patients who are clearly pigmented following recent exposure to the sun or a solarium.
- Patients treated with Roaccutane during the last six months.
- Patients who are not considered able to follow the treatment protocol (e.g. severely alcoholic patients, dementia patients, mentally ill patients, etc.).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Bispebjerg Hospital
🇩🇰Copenhagen, Copenhagen nv, Denmark