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临床试验/DRKS00017259
DRKS00017259尚未招募4 期

The effects of phenylephrine and norepinephrine on maternal and umbilical oxidative stress level during cesarean delivery under spinal anesthesia

Clinic of Gynaecology and Obstetrics University Clinical centre Nis0 个研究点目标入组 40 人开始时间: 2019年5月10日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
19 Years 至 35 Years(—)
性别
Female

入选标准

  • Patients ASA I and II status, scheduled for elective caesarean section in spinal anesthesia who have given written informed consent.

排除标准

  • Exclusion criteria include contraindications and patients’ refusal of spinal anesthesia, known cardiac, respiratory, neurologic, renal, endocrine, psychiatric disorders, history of drug or alcohol abuse, morbid obesity, preeclampsia, active labor, known fetal congenital abnormalities or signs of fetal compromise.

研究者

发起方
Clinic of Gynaecology and Obstetrics University Clinical centre Nis

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