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Recruiting
NCT05725213
ADL-PDT Under Routine Clinical Conditions in Patients With Actinic Keratosis
Conditions: Actinic Keratoses
Sex: All
Ages: 18 Years – N/A
Enrollment: 350
Sponsor: Galderma Laboratorium GmbH
Location: Germany
Summary
The objective of this non-interventional study (NIS) is to gain comprehensive insights into the practicability of ADL-PDT with Metvix® in patients with actinic keratoses under real-world conditions.
Eligibility Criteria
Inclusion Criteria:Written informed consent to participate in the studyAge ≥18 yearsThin or non-hyperkeratotic and non-pigmented actinic keratoses (AK) on the face or scalp (Olsen grade 1 or Olsen grade 2)The decision to undergo ADL-PDT with Metvix® was made independently of this studyNo contraindication (according to the SmPC)Exclusion Criteria:Hypersensitivity to the active substance or to one of the other ingredients listed in section 6.1 of the SmPC or other ingredients, including peanut oil, peanut or soy.Morphaeaform basal cell carcinomaPorphyriaPregnancy
Source: ClinicalTrials.gov (NCT05725213). StuddyBuddy aggregates publicly available trial information.