跳至主要内容
临床试验/ACTRN12611000909921
ACTRN12611000909921尚未招募1 期

Comparison of Postoperative Analgesic Effect of intrathecal clonidine and fentanyl added to bupivacaine in Patients undergoing cesarean section

Qazvin Medical Science University0 个研究点目标入组 90 人开始时间: 2011年8月24日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
90

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
18 Years 至 45 Years(—)
性别
Female

入选标准

  • patients with American Society of Anesthesiologists(ASA) physical status I and II, undergoing elective cesarean section

排除标准

  • significant coexisting disease such as hepato-renal and cardiovascular disease, any contraindication to regional anesthesia such as local infection or bleeding disorders, allergy to clonidine or fentanyl , long-term opioid use or a history of chronic pain.

研究者

发起方
Qazvin Medical Science University

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