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临床试验/ISRCTN72179764
ISRCTN72179764已完成不适用

An observer blind, parallel group, randomised multicentre study to compare the safety and efficacy of a new formulation of topical clindamycin phosphate in patients with mild to moderate acne

ProStrakan Pharmaceuticals (UK)0 个研究点目标入组 270 人开始时间: 2005年10月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
270

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Consenting patients of either sex, between 12 and 40 years of age, with mild to moderate inflammatory acne with a grade ranging from 2.0 to 7.0 (The Leeds Revised Acne Grading System, 1998).

排除标准

  • 1. Patients with significant nodulocystic acne
  • 2. Use of systemic topical antibiotics within 4 weeks prior to the start of treatment
  • 3. Concomitant medication which may interfere with study evaluation

研究者

发起方
ProStrakan Pharmaceuticals (UK)

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