Phase
Condition
Keratoses
Treatment
5FU-Calcipotriol
5-FU 50 MG/ML Topical Cream
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adults above 18 years of age
Clinical and dermoscopical diagnosis of AK by a dermatologist, in one or morearea(s):
Face, ears, (balding) scalp
Neck/Shawl area, including the sun-exposed chest area
Upper extremities
Number of AK lesions ≥4 in a continuous treatment area of up to 100 cm2
AK Olsen grade I-III
Exclusion
Exclusion Criteria:
Previous field treatment for AK within 2cm of the treatment area, within 3 months
(non) melanoma skin cancer in treatment area
Mucosal lesions
Genetic skin cancer disorder
Women who are pregnant or breastfeeding
Women of childbearing potential, who are not willing to use effective contraceptivemeasures
Previous allergy or intolerance to either 5FU or calcipotriol
Patients with known contra-indications for calcipotriol use: previous diagnosis ofhyper-calcemia, disturbed calcium metabolism, severe kidney or liver dysfunction
Concurrent use of oral capecitabine or any other topical or systemic chemopreventiveagent for any indication
Concurrent use of other topical treatments registered as treatment for AK
Limited understanding of the Dutch language and not being able to give informedconsent (incapacitated patients)
Study Design
Connect with a study center
Catharina Hospital Eindhoven
Eindhoven, Brabant 5623 EJ
NetherlandsActive - Recruiting
Zuyderland Medical Center
Heerlen, Limburg 6419 HC
NetherlandsActive - Recruiting
Maastricht University Medical Center
Maastricht, Limburg 6229 HX
NetherlandsActive - Recruiting
VieCuri Medical Center
Venlo, Limburg 5912 BL
NetherlandsActive - Recruiting


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