Assessment of Treatment Success and Quality of Life in Patients With Actinic Keratoses Under Therapy With Ingenol Mebutate in a Period of 8 Weeks
NCT02090465 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 840
Last updated 2019-12-17
Summary
Assessment of treatment success and quality of life in patients with actinic keratoses under therapy with Ingenol Mebutate (Picato) in a period of 8 weeks.
Conditions
- Actinic Keratosis
Interventions
- DRUG
-
Ingenol Mebutate
No intervention: observation of routine use of Picato®
Sponsors & Collaborators
-
LEO Pharma
lead INDUSTRY
Principal Investigators
-
Thomas Diepgen, Prof. Dr. med. · University Hospital Heidelberg
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-07-31
- Primary Completion
- 2013-12-31
- Completion
- 2013-12-31
Countries
- Germany
Study Locations
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