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临床试验/ACTRN12616000165482
ACTRN12616000165482已完成不适用

Post-dural puncture headache after cesarean section: Comparison with median and paramedian approaches

Konya Training and Research Hospital0 个研究点目标入组 200 人开始时间: 2016年2月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200

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
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
19 Years 至 45 Years(—)
性别
Female

入选标准

  • Two hundred pregnant, gestational age 38-40, between the ages of 19-45 yr, ASA physical status I, scheduled to undergo elective caesarean section under spinal anesthesia, were studied

排除标准

  • Exclusion criteria were contraindication to neuraxial anesthesia or known allergy to bupivacaine, spinal puncture failure, or a need for additional intraoperative analgesia, body mass index (BMI) >35 kg/m2, general anesthesia or epidural anesthesia, emergency CS and patients with chronic or postdural puncture headache history.

研究者

发起方
Konya Training and Research Hospital

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