L81.8
Conditions
Interventions
Group 1: One half ot the tattoo was treated with a standard nanosecond laser (694 nm). The laser was applied at regular time intervals of 4 weeks for up to eight treatments.
Group 2: The other half o
Sponsors
Klinik und Poliklinik für Dermatologie, Universitätsklinikum Regensburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: full legal age, written consent of the proband
Exclusion criteria
Exclusion criteria: pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tattoo clearance (primary endpoint) was appraised by physicians, blinded observers and by subjects. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain and adverse reactions (secondary endpoints) were appraised by physicians, blinded observers and by subjects. The extent and duration of adverse reactions were additionally assessed by using a questionnaire and photo-documentation between each consecutive treatment | — |
Countries
Germany
Contacts
Public ContactKatharina Weiß
Klinik und Poliklinik für Dermatologie, Universitätsklinikum Regensburg
Outcome results
None listed