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临床试验/NCT03327831
NCT03327831已完成4 期

UCI 14-92 / HS#2015-1889: Phase IV Study of Daylight Photodynamic Therapy With Aminolevulinic Acid for Actinic Keratoses

University of California, Irvine1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年4月最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
30
试验地点
1
主要终点
Percent Change in the Number of Actinic Keratoses

研究概览

简要总结

Photodynamic therapy is an effective treatment for actinic keratoses. In the United States topical aminolevulinic acid (ALA) is approved as a photosensitizing agent for this treatment, and it has traditionally been activated with the use of an in-office artificial light source. This clinical trial seeks to measure the safety and efficacy of using natural sunlight to activate the ALA.

详细描述

  • Initial Visit:

  • study inclusion criteria reviewed

  • consent forms reviewed

  • creation of facial map for actinic keratoses

  • face cleansed with chlorhexidine soap

  • light curettage of precancerous skin lesions

  • application of topical aminolevulinic acid (ALA)

  • application of sunscreen

  • patient then spends 2 hours outdoors in a shaded area

  • after treatment the patient is to remain indoors for 48 hours

  • 3 month follow up visit

  • facial map of actinic keratoses used to document treatment response
  • 6 month follow up visit

  • facial map of actinic keratoses used to document treatment response

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Clinical diagnosis of >10 actinic keratoses on head and neck
  • Age ≥ 18 years (Because no dosing or adverse event data are currently available on the use of topical aminolevulinic acid in patients <18 years of age, children are excluded from this study)
  • Ability to understand and the willingness to sign a written informed consent.

排除标准

  • Patients currently undergoing anti-neoplastic therapy including but not limited to the following:
  • Topical imiquimod
  • Topical 5-fluorouracil
  • Topical ingenol mebutate
  • Topical diclofenac
  • Topical retinoids
  • Oral acitretin
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to aminolevulinic acid
  • Patients with a known photosensitivity disorder including but not limited to porphyria, lupus, polymorphous light eruption, or immunobullous disease.
  • Patients taking known photosensitizing medications including but not limited to griseofulvin, thiazide diuretics, sulfonylureas, phenothiazines, sulfonamides and tetracyclines.
  • pregnancy

研究组 & 干预措施

Aminolevulinic Acid with daylight photodynamic therapy arm

Experimental

This study has a single, open label treatment arm. Patients will have topical aminolevulinic acid applied to the actinic keratoses in the treatment area (face/scalp) and will spend 2 hours outdoors in the shade to activate the medication. The patient then follow up in clinic 3 months and 6 months after their treatment to have the number of actinic keratoses counted.

干预措施: Aminolevulinic Acid (Drug)

结局指标

主要结局

Percent Change in the Number of Actinic Keratoses

时间窗: 0 (baseline) and 6 months

Percent change in number of actinic keratoses at 6 months

次要结局

  • Number of Participants With Adverse Events(2 days)

研究者

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

Christopher Zachary

Principal Investigator

University of California, Irvine

研究点 (1)

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