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临床试验/IRCT2013022112552N1
IRCT2013022112552N1已完成未知

Comparing the Analgesic Effects of Lidocaine Plus Buprenorphine and Lidocaine Alone In Women With Cesarean Section Under Spinal Anesthesia,Babol University of Medical Sciences

Babol Univesity of Medical Sciences0 个研究点目标入组 400 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
400

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
17 years 至 41 years(—)
性别
Female

入选标准

  • Inclusion Criteria: All pregnant women candidate for elective cesarean section, in ASA class I (American Society of Anesthesiology) aged 17-41 Years.

排除标准

  • Maternal or fetal contraindication for spinal anesthesia; Severe fetus distress; Emergency Cesarean; Addiction, Drug or OTC abuse, Using Anti-epileptic drugs, Blood pressure more than 140/90 mmHg, Gestational diabetes,Psychiatric problems; Uncontrolled co-existent internal disease

研究者

发起方
Babol Univesity of Medical Sciences

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