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临床试验/NCT00509886
NCT00509886已完成不适用

Non-prescription Versus Prescription Topical Treatments Versus no Treatment in the Control of Sweating

Northwestern University1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2007年6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
24
试验地点
1
主要终点
Gravimetric analysis

研究概览

简要总结

The purpose of this study is to assess the effectiveness of the prescription treatment compared to the non-prescription treatment. It is hypothesized that the prescription treatment will have a significantly greater effect than the non-prescription treatment on decreasing excess sweating.

详细描述

The objective of this study is to assess the effectiveness of the prescription treatment compared to the non-prescription treatment. It is hypothesized that the prescription treatment will have a significantly greater effect than the non-prescription treatment on decreasing excess sweating.

研究设计

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

入排标准

年龄范围
21 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • age 21-30 years
  • males and females
  • The subjects are in good health.
  • The subjects have willingness and the ability to understand and provide informed consent for participation in the study.

排除标准

  • Subjects with primary hyperhidrosis
  • Subjects who are unable to withstand prolonged heat exposure or who have self-reported history of cardiovascular or respiratory disorders.
  • Subjects who are unable to give informed consent.
  • Subjects with mental illness.
  • Subjects who are pregnant or nursing.
  • Subjects with systemic or local skin disease and/or infection that may interfere with the conduct of the study.

研究组 & 干预措施

1

Experimental

ARMs were randomized. One side of the body received treatment with one antiperspirant and the contralateral side with a different antiperspirant.

干预措施: Drysol (Drug)

2

Experimental

ARMs were randomized. One side of the body received treatment with one antiperspirant and the contralateral side with a different antiperspirant.

干预措施: Drioff (Drug)

结局指标

主要结局

Gravimetric analysis

时间窗: 3 hours

次要结局

  • HDSS(3 hours)
  • Subject sweat assessment(3 hours)

研究者

申办方类型
Other

研究点 (1)

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