跳至主要内容
临床试验/IRCT2013051612094N2
IRCT2013051612094N2已完成2 期

Comparison effect of intravascular administration of colloid versus crystalloid in prevention of hypotension after spinal anesthesia for cesarean section

Vice Chancellor for Research, Mashhad University of Medical Science0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100

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 years 至 40 years(—)
性别
All

入选标准

  • Candidates for elective cesarean surgery; ASA I-II; 18-40 years old.
  • Exclusion criteria: Patients who received intravenous fluids before entering the operating room; BMI=30; ASA>3; Age less than 18 years and more than 40 years; Contraindications to spinal anesthesia procedures; Emergency cesarean section; Amount of intraoperative bleeding over 1000cc; History of hypertension and blood pressure in pregnancy; Instances may increase the risk of bleeding and inertia.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research, Mashhad University of Medical Science

相似试验