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临床试验/IRCT20221011056143N1
IRCT20221011056143N1招募中2 期

The effect of rectal oxytocin suppositories compared to routine methods in reducing pain and bleeding after elective cesarean section - a randomized clinical trial

Karaj University of Medical Sciences0 个研究点目标入组 52 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
52

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
20 years 至 40 years(—)
性别
Female

入选标准

  • Pregnant women candidates for elective cesarean surgery for the second time
  • Age 20 to 40 years
  • Full-term women (37 full weeks of pregnancy and singletons) who undergo active cesarean section for non-emergency reasons.
  • A.S.A Class II
  • Not suffering from underlying diseases such as diabetes, high blood pressure, preeclampsia, eclampsia or a history of taking certain drugs.
  • Not suffering from hypothyroidism
  • Insensitivity to oxytocin
  • Absence of fetal anomalies
  • No history of headache and migraine
  • No history of taking psychotropic drugs
  • No alcohol or drug addiction
  • Complete mastery of official language conversation and the ability to read and write in Persian
  • No meningitis at the time of study
  • Not suffering from psychiatric diseases

排除标准

  • Severe drop in blood pressure during cesarean section
  • Any arrhythmia, whether tachyarrhythmia or bradyrhythmia
  • Heavy bleeding during cesarean section
  • Any disruption in the delivery process that prolongs the surgical process or repeats the caesarean section, including rupture of the bladder or bowels during surgery.
  • Hemodynamic changes during surgery, nausea and vomiting, respiratory arrest, arrhythmia and severe bleeding
  • The occurrence of shivering and severe pain in patients after surgery
  • The need for extra days of oxytocin or the need for other drugs such as metrogen and misopropylol

研究者

发起方
Karaj University of Medical Sciences

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