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临床试验/IRCT20091219002883N6
IRCT20091219002883N6招募中3 期

Comparison of pain intensity and intrathecal complications of 50 and 100 µg morphine with very low dose of naloxone in patients undergoing cesarean section

Mazandaran University of Medical Sciences0 个研究点目标入组 94 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
94

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

  • Age over 18 years
  • Pregnant women with prior planning for cesarean section without Majo disease
  • Absence of pregnancy-induced disease such as preeclampsia
  • Term twin pregnancy (37 to 42 weeks)
  • First or second pregnancy
  • Tendency to cesarean delivery by spinal anesthesia

排除标准

  • Dissatisfaction with participating in the study
  • Any contraindications to anesthesia with spinal technique
  • History of any idiocyncratic allergy or reaction to opioid drugs
  • Chronic pain syndrome or regular use of opioids
  • There is predictable evidence of anomaly in the fetus
  • Allergy or intolerance to ketorolac, ibuprofen or oxycodone • Body mass index above 40
  • Failure of spinal anesthesia
  • Prolongation of operation time

研究者

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