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临床试验/PACTR201706002303170
PACTR201706002303170已完成未知

Dexmedetomidine adminstration in Patients with Pre-eclampsia undergoing caeserian section

menoufiya faculty of medicine0 个研究点目标入组 60 人开始时间: 2017年5月19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
60

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

年龄范围
18 Year(s) 至 40 Year(s)(—)
性别
Female

入选标准

  • Patients included were 18-40 years, with gestational age ¿ 34 weeks and have mild pre-eclampsia with a systolic blood pressure < 160 mm Hg and a diastolic blood pressure < 110 mmHg and urinary protein dipstick + or 2+.

排除标准

  • Exclusion criteria included patient refusal to be included in the study, allergy to dexmedetomidine, body mass index >40kg/m2, systemic diseases (cardiac, pulmonary, hepatic, renal, neurological, neuromuscular, diabetes mellitus, anemia, coagulation disorders, bleeding disorders, seizures), HELLP syndrome, patients receiving anticoagulant or antipsychotic drugs, anti-partum hemorrhage, fetal distress and multiple pregnancy.

研究者

发起方
menoufiya faculty of medicine

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