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临床试验/NCT06337968
NCT06337968尚未招募不适用

Circum-Psoas Block for Arthroscopic Hip Surgery: a Randomized Trial

The Second Hospital of Shandong University0 个研究点目标入组 74 人开始时间: 2024年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
74
主要终点
pain severity at 6 hours postoperatively

研究概览

简要总结

Arthroscopic hip surgery is being increasingly performed to treat both intraarticular and extraarticular hip diseases. Despite the minimally invasive approach, patients undergoing arthroscopic hip surgery still suffer severe pain due to the complex nature of hip innervation. Postoperative pain reduces patient satisfaction and delay patient recovery and discharge. The efficacy of regional anesthesia techniques in postoperative pain management have been proved in various surgeries. However, it remains controversial whether or not peripheral nerve blocks can significantly improve postoperative analgesia after hip arthroscopy.

Several studies have shown that the fascia iliac block cannot improve postoperative analgesia for hip arthroscopy because it blocks only some branches of the lumbar plexus but not the sacral plexus. Circum-Psoas Block (CPB) which has been defined in recent years is able to block the lumbar plexus nerves as well as sacral plexus such as the sciatic, superior gluteal, and inferior gluteal nerves. Therefore, the investigators predict that it can provide effective postoperative analgesia for hip arthroscopy. In this study, the researchers aim to investigate the effectiveness of CPB in hip arthroscopy.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Primary unilateral ambulatory hip arthroscopy
  • Age 18 to 70 years
  • ASA physical status I to III
  • Ability to follow the protocol.

排除标准

  • Age <18 or >70 years of age
  • BMI above 40
  • Contraindications to peripheral nerve blockade
  • Pregnancy
  • Chronic pain condition requiring opioid intake at home
  • Allergy to opioids or local anesthetics
  • Patient refusal

结局指标

主要结局

pain severity at 6 hours postoperatively

时间窗: 6 hours postoperatively

Postoperative pain assessed with NRS pain score (NRS 0: no pain 10: pain as bad as can be) at 1, 6, 12, 24 hours postoperatively. However, to be more precise in our assessment, the effectiveness of each intervention was defined as a reduction in the pain at 6 hours postoperatively.

次要结局

  • Postoperative opioid consumption(up to the first 24 hours postoperatively)
  • Postoperative nausea and vomiting(up to the first 24 hours postoperatively)
  • neurologic evaluation(1, 6, 24 hours postoperatively)
  • Patient satisfaction(at the end of 24 hours postoperatively)

研究者

申办方类型
Other
责任方
Sponsor

相似试验

CPB for Arthroscopic Hip Surgery | 临床试验