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临床试验/TCTR20230919004
TCTR20230919004尚未招募4 期

Comparative study of the efficacy of ultrasound-guided transversus abdominis plane block between using 0.125% and 0.25% of bupivacaine on postoperative opioid consumption in kidney transplant recipients

Faculty of medicine, Khon Kaen University0 个研究点目标入组 76 人开始时间: 2023年9月19日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
入组人数
76

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
18 Years 至 65 Years(—)
性别
All

入选标准

  • 1.ESRD patients who undergoing KT recipients.
  • 2.Age at least 18 years old
  • 3.American society of Anesthesiologists (ASA PS) classification III-IV

排除标准

  • 1.History of chronic pain
  • 2.History of using analgesic medication within 24 hours
  • 3.Long term usage of antidepressants, antipsychotics, anticonvulsant, clonidine at least 3 months
  • 4.Known allergy to any study drugs
  • 5.Pregnancy or lactation
  • 6.Contraindicated for TAP block such as coagulopathy, skin infection
  • 7.Unable or refusal to use IV PCA

研究者

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