NCT lookup
Pull any trial record directly from ClinicalTrials.gov.
A Randomized Trial to Study Combined Pulsed Dye Laser and Rapamycin Treatment of Port Wine Stain Birthmarks.
A Randomized Trial to Study Combined Pulsed Dye Laser and Rapamycin Treatment of Port Wine Stain Birthmarks.
CompletedPhase 1
Sponsor: University of California, Irvine
Conditions: Port Wine Stain
Interventions: Rapamycin Treatment of Port Wine Stain
Countries: United States
The purpose of this study is to improve port wine stain therapeutic outcome in response to laser therapy. The researchers want to determine whether the combined use of pulsed dye laser therapy and rapamycin will improve PWS therapeutic outcome.
Eligibility overview
Sex: ALL
Age: 18 Years to —
Healthy volunteers: No
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * port wine stain birthmarks suitable for comparison testing. Exclusion Criteria: * Pregnancy. * Abnormal blood hematology or chemistry blood tests or urine analysis. * History of cancer, History of high cholesterol, lipids or liver disease * Allergy to macrolide drugs (e.g., erythromycin). * Any therapy within the previous two months to the proposed PWS treatment sites. * Concurrent use of known photosensitizing drugs,immunosuppressive drugs or systemic steroids,antifungals, antiepileptics, HIV protease inhibitors, cimetidine, cisapride, clarithromycin, dannzol, diltiazem, erythromycin, metoclopramide, rifabutin, rifampin, rifapentine, troleandomycin, or verapamil.
Locations (1)
- Irvine, California, United States