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临床试验/JPRN-UMIN000037783
JPRN-UMIN000037783已完成未知

Impact of the Intrapartum Synthetic Oxytocin Dose on Breastfeeding and Endogenous Oxytocin: Cohort study - Impact of the Intrapartum Synthetic Oxytocin Dose on Breastfeeding

St. Luke's International University0 个研究点目标入组 95 人开始时间: 2019年8月26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
95

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 43years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1) Cesarean delivery 2) Medical or pregnancy complications (hypertensive disorders of pregnancy, gestational diabetes (more than 2 points), uterine anomalies) 3) History of breast surgery 4) History of mental illness, epilepsy, cancer 5) Taking or inhaling steroids 6) HTLV, HIV, HBV, HCV positive 7) Smoker 8) Alcoholism 9) Illegal drug users 10) Bleeding in mouth (Periodontal disease, bleeding gums, stomatitis) 11) When epidural anesthesia is delivered without using synthetic oxytocin 12) Preterm birth (giving birth before 37 weeks of pregnancy) 13) Birth weight of less than 2500g 14) Oral anomalies in newborns 15) Apgar score of less than 7 at birth in newborns 16) Neonatal admission to NIC

研究者

发起方
St. Luke's International University

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