ISRCTN17618579已完成未知
Safety and efficacy of potential vaginal probiotics administrated orally in healthy volunteers
Tervisetehnoloogiate Arenduskeskus AS (Competence Centre on Health Technologies)0 个研究点目标入组 50 人开始时间: 2015年4月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 50
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
- Female
入选标准
- •1. Desire to participate
- •2. Age 18–50 years
- •3. Signed informed consent
- •4. Participants considered themselves 'healthy'
- •5. Screening blood tests (blood glucose, glycated haemoglobin, inflammatory indices, liver and kidney functional tests)
排除标准
- •1. Diabetes and acute infection
- •2. Food allergy
- •3. Use of any antimicrobial drug within past month
- •4. Current use of any regular concomitant medication, including medical preparations, non-steroidal anti-inflammatory drugs and antioxidant vitamins
- •5. Pregnancy or breastfeeding
- •6. History or clinical signs of cardiovascular abnormalities
研究者
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