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临床试验/IRCT20161126031095N3
IRCT20161126031095N3招募中2 期

Comparison of the effect of adding Dexamethasone and Fentanyl to Bupivacaine in transverse abdominal plane block (TAP) on pain intensity after cesarean section by spinal anesthesia in Sari Emam hospital in 1401

Mazandaran University of Medical Sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
入组人数
60

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 50 years(—)
性别
All

入选标准

  • Patients 18-50 years old
  • Patients undergoing cesarean section under spinal anesthesia
  • Patients with American Society of Anesthesiology (ASA) class I and II anesthesia status (ASA definition = healthy patient without organic, biochemical or mental disease and ASAII = patient with mild systemic disease such as mild asthma - controlled hypertension - disease has no effect on activity not daily - the possibility of affecting anesthesia and surgery)
  • Patients who can perceive and evaluate their pain on a visual analog pain scale. (VAS; scale 0-10)
  • They were eligible to provide written informed consent to enroll in the study
  • Body mass index kg/m2 = 23.9-18.5
  • Absence of coagulopathy
  • No alcohol or drug addiction

排除标准

  • Having chronic pain, or having underlying diseases such as moderate or severe heart, kidney, lung or nerve diseases, significant scoliosis or kyphosis, excessive obesity
  • Taking painkillers before surgery
  • Infection at the injection site
  • History of abdominal surgery or trauma
  • Respiratory tract infection within 2 weeks
  • New York Heart Association Class >II cardiac status and psychiatric disorders that interfere with pain perception and evaluation
  • They had a history of anaphylaxis using bupivacaine
  • Patients who did not tolerate spinal anesthesia well and had to be converted to general anesthesia for cesarean section
  • Individuals who could not provide informed consent or patients who did not wish to participate in the study

研究者

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