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临床试验/ISRCTN13247823
ISRCTN13247823
进行中(未招募)
未知

A randomised controlled trial comparing an individualised, height–related dose of intrathecal 0.5% hyperbaric bupivacaine with the standard fixed dose of 2.6 ml, for elective Caesarean section

County Durham and Darlington NHS Foundation Trust0 个研究点目标入组 200 人2023年2月22日

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Spinal anaesthesia for elective Caesarean section
发起方
County Durham and Darlington NHS Foundation Trust
入组人数
200
状态
进行中(未招募)
最后更新
3年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2023年2月22日
结束日期
2024年11月1日
最后更新
3年前
研究类型
Interventional
性别
Female

研究者

入排标准

入选标准

  • 1\. Height of \= 150cm and \= 160cm or \= 165cm and \= 175cm (rounded to nearest cm)
  • 2\. Elective Caesarean section
  • 3\. Singleton pregnancy
  • 4\. Gestation 36 weeks or greater
  • 5\. American Society of Anesthesiologists (ASA) physical status II (appendix 6\) with the exception for term BMI \= 40
  • 6\. No known foetal abnormalities

排除标准

  • 1\. Height \< 150 cm (rounded to nearest cm)
  • 2\. Height \> 175 cm (rounded to nearest cm)
  • 3\. Height \= 161 cm and \= 164 cm (rounded to nearest cm).
  • 4\. Age \< 18 years
  • 5\. Known or anticipated difficult airway
  • 6\. Term BMI \> 50
  • 7\. Anterior or posterior placenta praevia
  • 8\. ASA physical status III or greater (appendix 6\) with the exception for term BMI \= 40
  • 9\. Patients with pre \-existing (essential) hypertension or pregnancy –induced hypertension
  • 10\. Contraindication or refusal for spinal anaesthesia

结局指标

主要结局

未指定

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