Investigation of the Effect of a 2 Weeks Lipikar Urea 30% Application Preceding a Planned Topical 5-FU 4% Actinic Keratoses Treatment on Efficacy of 5-FU 4%
Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
This study is conducted in one center in Germany, in adult subjects having actinic keratoses (grade I or II) lesions on the scalp and meeting specific inclusion/exclusion criteria. The purpose of the study is to evaluate a holistic management (efficacy, tolerability and lesion cosmetic outcomes) of Tolak® treatment.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:
• diagnosis of at least 4 non-hypertrophic, non-hyperkeratotic actinic keratosis of the the scalp
• planned treatment of actinic keratoses of the scalp with Tolak®
• Olsen grade I or II
Locations
Other Locations
Germany
CentroDerm GmbH
RECRUITING
Wuppertal
Contact Information
Primary
Thomas Dirschka
s.weber@centroderm.de
+49 2 02 / 629337-32
Time Frame
Start Date: 2024-04-05
Estimated Completion Date: 2025-06
Participants
Target number of participants: 100
Treatments
Experimental: Group A: holistic approach
adult subjects having AK (grade I or II) lesions on the scalp and meeting specific inclusion/exclusion criteria including a Tolak® treatment planned before study start
Active_comparator: Group B: Tolak® Standard of use
adult subjects having AK (grade I or II) lesions on the scalp and meeting specific inclusion/exclusion criteria including a Tolak® treatment planned before study start
Related Therapeutic Areas
Sponsors
Leads: Cosmetique Active International