跳至主要内容
临床试验/CTRI/2024/02/063340
CTRI/2024/02/063340尚未招募4 期

Comparison of efficacy of intrathecal bupivacaine heavy (0.5%) and levobupivacaine heavy (0.5%) for elective caesarean section - Nil

Anagha V Harlapur0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

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

入选标准

  • Age 18-30 years
  • ASA grading I and II
  • Elective caesarean section surgical section

排除标准

  • Patient who refused to give consent.
  • A Documented sensitivity to drug in the past.
  • Bleeding diathesis and coagulopathy.
  • Age less than 18 and more than 30.
  • ASA grading III and IV.
  • Patient on anti hypertensive, anxiolytics, and anti epileptic.
  • Morbidly obese.
  • Patients for emergency lscs.
  • Patients with neurological and psychiatric illness.
  • Patients with spinal deformity.
  • Local site infections.

研究者

发起方
Anagha V Harlapur

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