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临床试验/NCT02019355
NCT02019355已完成早期 1 期

The Role of Calcipotriol in Treatment of Pre-cancerous Skin Lesions

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2013年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
132
试验地点
1
主要终点
percentage of change in the number of actinic keratoses from baseline

研究概览

简要总结

The main purpose of this study is to determine the effectiveness of a new combination therapy for actinic keratosis. This study investigates a new indication for an FDA-approved topical medication, calcipotriol, for treatment of actinic keratosis, including how well it works and how safe it is when used in combination with the standard of care medication (5-fluorouracil) for the skin condition.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age of at least 50 years
  • Presence of four to fifteen clinically typical, visible, and discrete actinic keratoses in 25 cm2 on any of the four anatomical sites: scalp, face, right upper extremity and left upper extremity
  • Ability and willingness of the patient to participate in the study (Informed consent is obtained)

排除标准

  • Treatment area is within 5 cm of an incompletely healed wound or a suspected basal-cell or squamous-cell carcinoma
  • Treatment area contained hypertrophic and hyperkeratotic lesions, cutaneous horns, or lesions that had not responded to repeated cryotherapy
  • Recent (within a month) use of medications that could interfere with evaluation of the treatment area (e.g., topical medications, artificial tanners, immunosuppressive medications, immunomodulating agents, cytotoxic drugs, ultraviolet B phototherapy, other therapies for actinic keratoses, or oral retinoids)
  • Premenopausal Women (to avoid any risk of pregnancy)
  • History of hypercalcemia or clinical evidence of vitamin D toxicity

研究组 & 干预措施

calcipotriol plus 5-fluorouracil

Experimental

calcipotriol 0.005% ointment and 5-fluorouracil 5% cream are mixed at 1:1 weight ratio. The compounded medication is applied topically twice a day for 4 days.

干预措施: 5-fluorouracil 5% cream (Drug)

calcipotriol plus 5-fluorouracil

Experimental

calcipotriol 0.005% ointment and 5-fluorouracil 5% cream are mixed at 1:1 weight ratio. The compounded medication is applied topically twice a day for 4 days.

干预措施: Calcipotriol 0.005% ointment (Drug)

5-fluorouracil plus vaseline

Active Comparator

5-fluorouracil 5% cream and vaseline are mixed at 1:1 weight ratio. The compounded medication is applied topically twice a day for 4 days.

干预措施: 5-fluorouracil 5% cream (Drug)

5-fluorouracil plus vaseline

Active Comparator

5-fluorouracil 5% cream and vaseline are mixed at 1:1 weight ratio. The compounded medication is applied topically twice a day for 4 days.

干预措施: Vaseline (Drug)

结局指标

主要结局

percentage of change in the number of actinic keratoses from baseline

时间窗: 8 weeks

To compare the efficacy of topical 5-fluorouracil+calcipotriol vs. 5-fluorouracil alone in treatment of actinic keratosis in patients with multiple actinic keratoses at each of the four anatomical sites (scalp, face, right upper extremity and left upper extremity). The outcome of interest is percentage change from baseline number of actinic keratoses in the target treatment area on scalp, face, right upper extremity and left upper extremity at 8 weeks after treatment.

次要结局

  • complete and partial (>75%) clearance of actinic keratoses(8wks)
  • Composite score of erythema, itching and skin pain after topical 5-fluorouracil+calcipotriol vs. 5-fluorouracil alone treatment of actinic keratoses(4days)
  • Induction of TSLP expression in keratinocytes by calcipotriol(4 days)
  • differences in response to topical 5-fluorouracil+calcipotriol vs. 5-fluorouracil alone between the four anatomical sites(8wks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lynn Cornelius, MD

Chief, Division of Dermatology

Washington University School of Medicine

研究点 (1)

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