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RECRUITING
NCT06274320
NA

Effect of Lipikar Urea 30% Before Actinic Keratoses Treatment

Sponsor: Cosmetique Active International

View on ClinicalTrials.gov

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.

Official title: 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%

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2024-04-05

Completion Date

2025-06

Last Updated

2024-06-18

Healthy Volunteers

Yes

Interventions

OTHER

Group A: holistic approach

2-week Lipikar Urea 30% application (once daily in the evening) + 4-week Tolak® treatment (once daily in the evening)

OTHER

Group B: Tolak® Standard of use

4-week Tolak® alone treatment (once daily in the evening)

Locations (1)

CentroDerm GmbH

Wuppertal, Germany