NCT01477879已完成1 期
Phase II Clinical Trial of Versabase/Sarracenia Purpurea Versus Placebo
Naturopaths International2 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2011年1月1日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 33
- 试验地点
- 2
- 主要终点
- Pain
研究概览
简要总结
This study will compare efficacy of versabase gel with 20% sarracenia purpurea versus placebo applied every 3-4 hours to herpes lesions.
详细描述
Patients screened for hsv one or two. Patients with herpes given a 1/8 oz of gel. Researcher does not know which is active and which is placebo (placebo is actually just versabase gel). Patent applies gel to lesions every 3-4 hours. Returns to clinic on days 3, 5, and 14 for evaluation. Up to 50 patients may be enrolled.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- •No active lesions
结局指标
主要结局
Pain
时间窗: 2 weeks
Pain scale-- subjective
Size
时间窗: 2 weeks
Measure lesion size over 2 weeks
次要结局
- Appearance(2 weeks)
研究者
Dr. Brandie Gowey, NMD
Brandie Gowey
Naturopaths International
研究点 (2)
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