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临床试验/DRKS00015114
DRKS00015114已完成4 期

The effects of remifentanil on maternal hemodynamic, oxidative stress and neonatal outcome: comparison of two dosing regimens used during the induction-delivery period of caesarean section performed under general anesthesia - Maternal and fetal effects of remifentanil used during caesarean section

Clinic of Gynaecology and Obstetrics University Clinical Center Nis0 个研究点目标入组 60 人开始时间: 2018年7月30日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
60

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 general anesthesia who have given written informed consent.
  • All patients refuse or have absolute/relative medical contraindications to regional anesthesia.

排除标准

  • Exclusion criteria are: known cardiac, respiratory, neurologic, renal, endocrine, psychiatric disorders, history of drug or alcohol abuse, morbid obesity, preeclampsia, predicted difficult airway management, active labor, known fetal congenital abnormalities or signs of fetal compromise.

研究者

发起方
Clinic of Gynaecology and Obstetrics University Clinical Center Nis

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