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临床试验/ACTRN12626000848303
ACTRN12626000848303进行中(未招募)不适用

Pain and opioid usage in hamstring tendon anterior cruciate ligament reconstruction with adductor canal block versus IPACK block: a single-centre randomised controlled trial

Northern Sydney Local Health District0 个研究点目标入组 100 人开始时间: 2026年7月31日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
16 Years 至 75 Years(—)
性别
All

入选标准

  • Aged 16 to 75 years.
  • American Society of Anaesthesiologists physical status grade I or II.
  • Undergoing primary anterior cruciate ligament reconstruction using hamstring tendon autograft.
  • Able to provide informed consent.
  • Undergoing surgery at Hornsby Hospital.

排除标准

  • Revision anterior cruciate ligament reconstruction.
  • Known allergy or contraindication to local anaesthetics, opioids, or study medications.
  • Chronic opioid use within the preceding 3 months.
  • Coagulopathy or bleeding disorder.
  • Severe hepatic or renal impairment.
  • History of alcohol or substance use disorder.
  • Inability to comply with study procedures or follow-up.
  • Refusal or inability to provide informed consent.

研究者

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