ISRCTN03397663已完成不适用
Evaluation of the efficacy and safety of a Sheabutter extract on cold sores (herpes simplex labialis)
BSP Pharma A/S (Denmark)0 个研究点目标入组 160 人开始时间: 2005年7月5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
- 160
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
- •Subjects aged 18 and 75 years, in good general health who have a clinical history of recurrent herpes labialis, with at least six self reported episodes of herpes lesion in the past year and at least one recurrance every three months.
排除标准
- •1. History of immunodeficiency
- •2. Use of other antiviral agents (including herbal medications), anti-inflammatory medications, steroids or analgesics during the treatment period
- •3. Known allergy to Sheabutter
- •4. Liver function tests greater than 3 times the upper limit of normal at baseline
- •5. Female participants who are lactating, pregnant or planning to become pregnant
- •6. Participants who have participated in another clinical trial in the last 30 days
- •7. Participants unwilling to comply with the study protocol
- •8. Any other condition, which in the opinion of the investigators could compromise the study
研究者
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