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临床试验/IRCT2017080635524N1
IRCT2017080635524N1已完成2 期

Comparing thr efficacy of topical 1 % clindamycin phosphate and niosomal clindamycin phosphate 1% solusion in reduction of acne vulgaris lesions

Vice Chancellor for research of Kerman University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100

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

年龄范围
12 years 至 30 years(—)
性别
All

入选标准

  • Mild to moderate acne vulgaris; Both male and female;age (12-30years); lack of treatment during the one month period before the study
  • exclusion criteria: pregnancy; breast feeding; hypersensitivity to clindamycin; history of inflamatory bowel disease(IBD); history of neuromuscular junction blocker using; history of systemic retinoid using in the past 6 month; history of oral estrogen using in the past 3 month; history of topical retinoid and oral antibiotic using in the past 1 month; history of antimicrobial soap and comedogenic products using in the past 2 weeks; history of astringents and abrasive products using in the past 1 week; hirsutism; androgenetic alopecia; Polycystic ovarian syndrome.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research of Kerman University of Medical Sciences

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