跳至主要内容
临床试验/NCT00667225
NCT00667225已完成不适用

Efficacy of Cantharidin in Molluscum Contagiosum: A Randomized, Blinded, Placebo-Controlled Prospective Study

University of North Carolina, Chapel Hill1 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2008年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
29
试验地点
1
主要终点
Patients Experiencing Complete Clearance of All Molluscum Lesions.

研究概览

简要总结

The University of North Carolina Department of Dermatology is conducting a clinical trial to evaluate a drug called cantharidin in the treatment of molluscum contagiosum. Molluscum is a common dermatologic disorder caused by a poxvirus. Molluscum typically presents with many flesh-colored bumps on the skin. It goes away on its own, though can last several months to several years. Cantharidin is a topical medicine which is applied at the clinic visit. It is well tolerated by the majority of children.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
5 Years 至 10 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Anyone aged 5-10 years with the clinical diagnosis of molluscum contagiosum.

排除标准

  • Anyone with immunosuppression including HIV or previous organ transplantation.
  • Anyone taking immunosuppressive medications.
  • Anyone who has previously received treatment with cantharidin.
  • Any female who has had her first menstrual period.

研究组 & 干预措施

I

Placebo Comparator

Subjects in this group will have topical application of cantharidin's vehicle at each visit.

干预措施: cantharidin's vehicle (Drug)

II

Experimental

Subjects in this group will have topical application of cantharidin at each visit.

干预措施: Cantharidin 0.7% (Drug)

结局指标

主要结局

Patients Experiencing Complete Clearance of All Molluscum Lesions.

时间窗: Baseline compared to 8 weeks (5 visits)

次要结局

  • Mean Change in Each Group Measured by Lesion Count.(Baseline compared to 8 weeks (5 visits))

研究者

申办方类型
Other

研究点 (1)

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