NCT00237978Unknown4 期
Control of Therapy of Acne Papulopustulosa by Visible Light With Waterfiltered Infrared and / or Adapalen (Differin Gel)
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- reduction of inflammatory and non-inflammatory lesions within 8 weeks after start of therapy
研究概览
简要总结
The aim of the study is to investigate the effectivity of visible light in combination with waterfiltered infrared in treating acne papulopustulosa. The reduction of inflammatory and non-inflammatory lesions within 8 weeks will be measured and compared with the standard treatment with Adapalene.
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
- None
入排标准
- 年龄范围
- 14 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Mild to moderate acne papulopustulosa according to Burton Scale Stage 3 to 4
- •At least 5 inflammatory and 5 non-inflammatory lesions in the face
- •Age >= 14 years
排除标准
- •pregnant and nursing women
- •Antiandrogen therapy
- •therapy with antibiotics within the last 4 weeks
- •therapy with retinoids within the last 6 months
- •natural or artificial UV-therapy within the last 4 weeks
- •severe acne papulopustulosa according to Burton Scale 5 or 6
- •Severe systemic condition
- •Secondary acne
研究组 & 干预措施
1
Active Comparator
VIS and wIRA
干预措施: VIS and wIRA (Radiation)
2
Active Comparator
VIS, wIRA and Adapalen
干预措施: Adapalen (Drug)
2
Active Comparator
VIS, wIRA and Adapalen
干预措施: VIS and wIRA (Radiation)
3
Active Comparator
Adapalen
干预措施: Adapalen (Drug)
结局指标
主要结局
reduction of inflammatory and non-inflammatory lesions within 8 weeks after start of therapy
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
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