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临床试验/CTRI/2024/05/067399
CTRI/2024/05/067399尚未招募3 期

Intrathecal hyperbaric bupivacaine versus hyperbaric ropivacaine in spinal anaesthesia in caesarean sections: a randomised control trial in a teaching hospital in northeast India. - Nil

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试验速览

阶段
3 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

  • i.All patients who will be registered for elective caesarean delivery and belonging to ASA (American Society of Anesthesiologists) grade I & II only.
  • ii.Patients between 145to 165 cms of height.
  • iii.Patients who will give valid informed written consent.
  • iv.Pregnancy over 37 weeks and less than 42 weeks.
  • v.Patient with weight of 45-95kgs.
  • vi.Patients with age between 18years and 40 years.

排除标准

  • i.Patient with abnormalities and problems in the embryo.
  • ii.Patient with indication of an emergency caesarean section.
  • iii.Patients having history of hypersensitivity to anesthetic agents.
  • iv.Infection at the subarachnoid block injection site.
  • v.Pre-term and post term delivery.
  • vi.ASA class higher than II.

研究者

发起方
eon

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