Acne Vulgaris Clinical Trial
Official title:
Epiduo in the Long-term Treatment of Moderate to Severe Acne With or Without Concomitant Medication
This observational study is designed to assess the long-term efficacy and safety of Epiduo (alone or in combination with other drugs) under daily clinical practice conditions in patients with moderate to severe inflammatory acne. In addition, the effect of Epiduo on quality of life and patient adherence will be assessed under marketed conditions.
This observational study is designed to assess the long-term efficacy and safety of Epiduo
under daily clinical practice conditions. The study includes patients of all ages with
moderate to severe inflammatory acne, taking Epiduo alone or in combination with other
drugs. In addition, the effect of Epiduo alone or in combination with other drugs on quality
of life and patient adherence will be assessed under marketed conditions.
The observational study is designed as a multicentre study, covering all parts of Germany.
Participating investigators are dermatologists with an adequate patient pool of acne
patients. The observation time per patient will be 9 months. An interim and final
examination with subsequent documentation are designated to be performed about 3 and 9
months after the start of treatment, respectively.
;
Observational Model: Cohort, Time Perspective: Prospective
| Status | Clinical Trial | Phase | |
|---|---|---|---|
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