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临床试验/IRCT20230403057808N1
IRCT20230403057808N1招募中3 期

Comparison of intrathecal injection of fentanyl and sufentanil along with bupivacaine in the onset, duration and quality of painless labor; A randomized double-blind clinical trial

Rasht University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
80

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 no limit(—)
性别
Female

入选标准

  • Primiparous or multiparous pregnant mothers with term pregnancy
  • Single fetus
  • American Society of Anesthesiologists' (ASA) classification I, II
  • In the advanced stage of labor with cervical dilation at least 5 centimeter in Primiparous and at least 4 centimeter in multiparous mothers
  • Age more than 18 years
  • Tending to have painless labor

排除标准

  • Refusal to participate in the study by pregnant mothers
  • Endocrine disease
  • Allergy to study drugs
  • Regional anesthesia contraindications such as coagulopathy, high intracranial pressure and infection of injection site .

研究者

发起方
Rasht University of Medical Sciences

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