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临床试验/NCT01213199
NCT01213199已完成2 期

Efficacy and Safety of Adapalene Gel 0.3% in the Treatment of Atrophic Acne Scars. A Pilot Study.

Galderma R&D1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2011年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Galderma R&D
入组人数
20
试验地点
1
主要终点
Global Scarring Severity

研究概览

简要总结

The purpose of this study is to assess the efficacy and safety of Adapalene Gel 0.3% in the treatment of atrophic acne scars.

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 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female subjects of any race, aged 18 to 50 years inclusive
  • Subjects with a past history of acne and with moderate to severe facial atrophic acne scars

排除标准

  • Subjects with active inflammatory acne lesions
  • Subjects with hypertrophic acne scars

研究组 & 干预措施

Differin 0.3%

Experimental

Differin® 0.3% Gel

Adapalene 0.3%

Topical to the face, once daily application in the evening for the first four weeks and twice daily application in the morning and in the evening for the following 20 weeks.

干预措施: Adapalene (Drug)

结局指标

主要结局

Global Scarring Severity

时间窗: Week 24

Grade Level: 1. Macular disease 2. Mild disease 3. Moderate disease 4. Severe disease

次要结局

未报告次要终点

研究者

发起方
Galderma R&D
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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