ISRCTN63012285已完成不适用
A randomised controlled study to compare efficacy and safety of chlorhexidine powder versus dry care in umbilical cord care of the newbor
Riemser AG (Germany)0 个研究点目标入组 670 人开始时间: 2005年10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
- 670
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
- •1. Healthy newborns on the first day of life
- •2. Gestational age: 37-42 weeks
- •3. Birth weight >2500 g
- •4. Informed consent given in a written form by both parents after being provided with detailed information about the nature, risks, and scope of the clinical trial as well as the expected desirable and adverse effects of the drug
排除标准
- •1. Current participation in another clinical trial
- •2. Signs of clinically relevant illnesses (excluding physiological neonatal hyperbilirubinemia)
- •3. Evidence for HIV- or Hepatitis B/C-infection
- •4. Evidence for infection of the newborn (also expected antibiotic therapy)
- •5. Treatment of the subject with systemic antibiotics
- •6. Treatment of the umbilical cord with local antimicrobial regimen before randomization
- •7. Twins or triplets
- •8. Delivery at home
- •9. Legal incapacity and/or other circumstances rendering the subjects parents unable to understand the nature, scope and possible consequences of the study
- •10. Unreliability or lack of cooperation from the parents
- •11. Any other condition which, in the opinion of the investigator, would render the subject ineligible for the study
研究者
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