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临床试验/IRCT2016120431225N1
IRCT2016120431225N1已完成未知

Comparison of the duration of analgesia following two method of posterior and lateral transverse abdominal blocks under ultrasound guidance after cesarean section

Vice Chancellor for research of Iran University of Medical Sciences0 个研究点目标入组 76 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
76

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 50 years(—)
性别
Female

入选标准

  • 18-50 year old females who are candidate for spinal anesthesia for elective and emergency cesarean section due to fetal distress; patients with ASA 1 & 2. Exclusion criteria: patients with ASA>3 & 4; contraindication for the use of spinal anesthesia; Emergent conditions due to organic problems such as eclampsia, preeclampsia, placenta previa and ...; history of allergy to bupivacaine; receiving an analgesic; BMI> 40; pre-pregnancy weight less than 50 kg; patients with an underlying disease or history of renal or liver disease or coagulopathy; prediction of spinal anesthesia unsuccessfulness (including inadequate anesthetic level); patients who have received sedation drugs fentanyl 100 macrograms and midazolam 2 miligrams during the procedure.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research of Iran University of Medical Sciences

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