Topical Imiquimod in Conjunction With Nd:YAG Laser for Tattoo Removal
Completed · Phase 1
Conditions studied: Healthy
In brief
The purpose of this study is to evaluate the efficacy of tattoo removal using topical imiquimod, 5% cream in conjunction with the 1064nm Nd:YAG laser. This procedure for tattoo removal will be compared to a laser removal alone.
Key facts
- Study ID
- NCT00638651
- Run by
- University of Miami
- People needed
- 3
- Starts
- 2008-02-01
- Expected to finish
- 2014-08-01
- Last updated by the study team
- 2018-03-22
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 2 tattoos no larger than 25cm2, professionally made, with approximately the same age, containing blue/black ink.
You may not qualify if…
- Hypersensitivity to imiquimod
- Current sun tan
- Use of vitamin E, non-steroid anti-inflammatory drugs, coumadin or aspirin for the past 10 days
- Amateur tattoos
- Pregnancy
- Breast-feeding status
- Immunosuppression
- Auto-immune diseases.
Where it is running
- Mohs, Dermatologic and Laser Surgery — Miami, Florida, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.