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临床试验/ISRCTN17618579
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

发起方
Tervisetehnoloogiate Arenduskeskus AS (Competence Centre on Health Technologies)

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