MedPath

Gene and Protein Expression Profiles After Treatment of Actinic Keratoses

Phase 2
Recruiting
Conditions
Actinic Keratoses
Interventions
Registration Number
NCT05740969
Lead Sponsor
Ismail Gögenur
Brief Summary

The primary aim of this study is to investigate the effect of 5-fluorouracil, imiquimod, and melatonin for actinic keratosis on immunological gene, and protein expressions profiles. Secondarily, the aim is to assess the effect of the treatment on the histopathology of actinic keratoses.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
48
Inclusion Criteria
  • Participants should have a clinical diagnosis of actinic keratosis
  • Participants should be 18 years old or above
  • Participants must sign an informed consent
Exclusion Criteria
  • Known allergic reaction to either 5-fluorouracil , imiquimod, or melatonin
  • Immunomodulating treatment
  • Predictable poor compliance (due to i.e. dementia, substance abuse, psychiatric disease, life-threatening disease or language barriers)
  • Pregnant or breastfeeding
  • Females not in menopause (defined as no menstruation during the last 12 months) should use a secure birth control (intrauterine devices, hormonal contraceptives including - oral pills, patches, vaginal rings and injections) during the entire period of the trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
MelatoninMelatoninPatients will be asked apply a 25 mg/g creme containing melatonin once a day on their lesion for 10 days. A biopsy will be taken four days after last application. The patient will be refered to a dermatologist for further treatment, if necessary.
ImiquimodImiquimodPatients will be asked apply a 50 mg/g creme containing imiquimod thrice a week on their lesion for 10 days. A biopsy will be taken four days after last application. The patient will be refered to a dermatologist for further treatment, if necessary.
5-Fluorouracil5FluorouracilPatients will be asked apply a 40 mg/g creme containing 5-Fluorouracil once a day on their lesion for 10 days. A biopsy will be taken four days after last application. The patient will be refered to a dermatologist for further treatment, if necessary.
Primary Outcome Measures
NameTimeMethod
Gene and protein expression profiles10 days of treatment
Secondary Outcome Measures
NameTimeMethod
histopathological assessment of actinic keratoses10 days of treatment

Trial Locations

Locations (1)

Zealand University Hospital

🇩🇰

Roskilde, Region Sjælland, Denmark

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