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临床试验/CTIS2024-511409-42-00
CTIS2024-511409-42-00进行中(未招募)1 期

Combination therapy of 5-Fluorouracil and Calcipotriol versus 5-Fluorouracil in the treatment of Actinic Keratosis: a multicentre randomized controlled clinical trial

niversity Hospital Maastricht0 个研究点目标入组 232 人开始时间: 2024年3月13日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
232

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Adults above 18 years of age, Clinical and dermoscopical diagnosis of AK by a dermatologist, in one or more area(s): Face, ears, (balding) scalp OR Neck/Shawl area, including the sun-exposed chest area OR Upper extremities, Number of AK lesions =4 in a continuous treatment area of up to 100 cm2, AK Olsen grade I-III

排除标准

  • 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, Previous allergy or intolerance to either 5Fluorouracil or calcipotriol, Patients with known contra-indications for calcipotriol use: previous diagnosis of hyper-calcemia, disturbed calcium metabolism, severe kidney or liver dysfunction, Concurrent use of oral capecitabine or any other topical or systemic chemopreventive agent for any indication, Limited understanding of the Dutch language and not being able to give informed consent

研究者

发起方
niversity Hospital Maastricht

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