跳至主要内容
临床试验/CTRI/2023/11/059394
CTRI/2023/11/059394尚未招募Phase 3 4

Comparison of postoperative pain relief with single shot adductor canal block with or without infiltration between popliteal artery and capsule of knee block for patients undergoing knee arthroscopy.

Government medical college and hospital1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年6月11日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
24
试验地点
1
主要终点
rescue fentanyl consumption

研究概览

简要总结

Pain due to knee arthroscopic surgeries leads to diff in early ambulation and increased opioid use. Therefore, regional anaesthesia techniques are being increasing used to treat postoperative pain . Adductor canal block has the disadvantage of being unable to alleviate posterior knee pain . The study is designed to compare the effect of ultrasound guided adductor canal block plus IPACK versus ultrasound guided adductor canal block alone for postoperative analgesia in patients undergoing knee arthroscopic surgeries.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 1 Age between 18 to 65 years 2 American society of anaesthesiologists (ASA) physical status 1 and 2 3.BMI 18 to 30 kg/m2 4 patients scheduled for knee arthroscopy.

排除标准

  • 1 patients refusing to give informed consent 2 patients with history of relevant drug allergy 3 patients with history of psychiatric illness and substance abuse 4 patients with severe cardiovascular respiratory metabolic or neurological disorders 5 pregnant and lactating women 6 patients with coagulopathy and bleeding disorders 7 infection at planned injection site 8 patient on steroids.

结局指标

主要结局

rescue fentanyl consumption

时间窗: 4 hour, 12 hour, 24 hour

次要结局

  • Patient satisfaction on 0- 100 VAS(4 12 24 hours after administration of block)
  • Sensory and motor blockade(4 12 24 hours after administration of block)
  • Time to first rescue analgesia
  • Pain scores on NRS(4 12 and 24 hours after administration of block)
  • Side effects(4 12 24 hours after administration of block)

研究者

发起方
Government medical college and hospital
申办方类型
Government medical college

研究点 (1)

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