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临床试验/PACTR201604001549201
PACTR201604001549201已完成未知

A RANDOMISED CONTROLLED TRIAL INVESTIGATING THE EFFECT OF ADDING FENTANYL TO LOW DOSE BUPIVACAINE IN COMBINED SPINAL-EPIDURAL ANAESTHESIA, USING EPIDURAL VOLUME EXTENSION TECHNIQUE IN CESAREAN SECTION.

Aga Khan University Hospital0 个研究点目标入组 44 人开始时间: 2016年3月26日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
44

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 50 Year(s)(—)
性别
Female

入选标准

  • All obstetric patients coming in for elective caesarean section in Aga Khan University Hospital Nairobi, who were;
  • Patients willing to participate in the trial having completed a fully signed informed consent.
  • American Society of Anesthesia class I or II patients.

排除标准

  • Emergency caesarean section patients
  • ASA III and IV patients
  • Patients with coagulation disorders
  • Patient refusal

研究者

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