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Pilot Study Evaluation of a Combination of Topical 5-Fluorouracil [5FU] and Calcipotriol in the Treatment of Cutaneous Actinic Keratosis [AK] and Intraepidermal Carcinoma [IEC] Lesions

Phase 2
Conditions
Skin cancer precursors
Skin - Dermatological conditions
Skin - Other skin conditions
Registration Number
ACTRN12621001242819
Lead Sponsor
Dr Leith Banney
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

Adults aged 18-85 years.
Extensive solar damage to skin over the face, as determined by a dermatologist.
Ability to comply with treatment regime as determined by the treating investigator.
Ability to undertake written informed consent prior to initiation of study protocol.
Ability/willing to attend follow up clinic visits that will include clinical photography.
Able to complete study surveys.

Exclusion Criteria

Patients commencing acitretin, other oral or topical retinoids or oral vitamin B3 in the past 3 months and for the duration of the study.
Patients with known allergy/hypersensitivity to 5FU cream.
Patients with known dihydropyrimidine dehydrogenase (DPD enzyme) deficiency.
Patients who are pregnant or breastfeeding. Female participants should avoid pregnancy and breastfeeding during use of treatment cream until three-month review.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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