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临床试验/PACTR202404650060916
PACTR202404650060916尚未招募Unknown

Post Caesarean Section Analgesia: A Comparative Study of Double Versus Triple Drug Combinations for Post Caesarean Section Analgesia at the Federal Medical Centre, Abuja- A Triple Blind Randomized Controlled Study.

未提供0 个研究点目标入组 234 人开始时间: 2024年2月5日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
入组人数
234

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
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • Pregnant women aged = 18 years who are booked for, and have given consent, for elective or emergency caesarean section procedure under spinal anaesthesia at term in the hospital.

排除标准

  • . Refusal to give consent
  • 2. History of opioid dependency
  • 3. Cardio-pulmonary depression
  • 4. History of chronic kidney or liver disease
  • 5. Known allergy to pentazocine, diclofenac and acetaminophen
  • 6. Delirium
  • 7. General anaesthesia
  • 8. Prematurity
  • 9. Intra uterine fetal death
  • 10. Prolonged surgery greater than 2 hours
  • 12. Sickle cell disease
  • 13. Any adverse fetomaternal outcome e.g. ICU or NICU admission.

研究者

发起方
未提供

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