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临床试验/CTRI/2022/12/048547
CTRI/2022/12/048547尚未招募未知

Comparison of Efficacy of intrathecal tramadol versus intrathecal fentanyl as adjuvant to 0.5% Bupivacaine for post operative pain relief in elective cesarean section - Not applicable

College of medicine and Sagore Dutta Hospital0 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
未知
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

  • Pregnant mothers of age 20 to 40 years
  • ASA Grade II.
  • Enrolled for elective caesarean section

排除标准

  • Age below 20 or above 40 years
  • Infection at site of injection, any coagulopathy disorder or patients on anticoagulants, pre-existing neurological disease, psychological troubles, endocrinal disease
  • Morbid obesity.
  • Failure of spinal blockade.
  • Patients with previous spinal surgery, kyphoscoliosis or any spinal deformity
  • Emergency CS.
  • Complicated pregnancy.
  • Intrauterine fetal compromise
  • Patients with known history of previous opioids abuse or allergic to opioids, allergy to local anaesthetic drugs,
  • History of any neurological disease like Gullion Berry syndrome, sub-acute combined degeneration of spinal cord etc.

研究者

发起方
College of medicine and Sagore Dutta Hospital

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