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临床试验/IRCT2013022512593N1
IRCT2013022512593N1已完成未知

A comparison of the effects of diclofenac sodium suppositories, intravenous paracetamol and the combination of diclofenac sodium suppositories and intravenous paracetamol on reducing the acute pain and the need to narcotic pain relievers after cesarean surgery under spinal anesthesia

Ahvaz Jundishapur University of Medical Sciences (AJUMS)0 个研究点目标入组 99 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
99

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 45 years(—)
性别
Female

入选标准

  • Being in ASA class 1 or 2; Being in ages between 18-35; Being first or second pregnancy.
  • Exclusion criteria: Having any known allergies and sensitivities, banned from narcotic drugs, paracetamol, and NSAIDs; Hepatic Dysfunction (transaminaze twice than upper limit of normal level); Kidney dysfunction (plasma creatinine higher than 2.5 mg/dl); Smoking or having any previous pulmonary disease; Drug, narcotic, and alcohol abuse; Subjects with the history of depression or chronic anxiety;Subjects experienced the side effects of spinal anesthesia: back pain, radicular pain, paresthesia and hypoesthesia, PDPH; Spinal contraindication; Contraindications for the Use of Spinal Anesthesia (Patient decline, infection in the spot for entering the needle, high intracranial pressure, bleeding susceptibility).

排除标准

  • 未提供

研究者

发起方
Ahvaz Jundishapur University of Medical Sciences (AJUMS)

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