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临床试验/NCT04322760
NCT04322760已完成不适用

Effect of Lidocaine 5% Patch Supplementation to Intra-articular Bupivacaine Dexmedetomidine After Arthroscopic Knee Surgery Under General Anesthesia

Tanta University0 个研究点目标入组 40 人开始时间: 2016年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
40
主要终点
The total dose of postoperative pethidine consumption

研究概览

简要总结

Surgery of the knee is a very common procedure which can be very painful and sufficient postoperative pain treatment is often problematic. The aim of this work was to study the effects of supplementation of intra-articular bupivacaine dexmedetomidine with lidocaine 5% patch after arthroscopic knee surgery under general anesthesia and its role in improving quality of anesthesia.

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
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients
  • ASA I & II
  • Aged between 18 to 60 years
  • Weight between 60 to 100 kg
  • Scheduled for elective arthroscopic knee surgery

排除标准

  • patient refusal.
  • history of cardiac disease.
  • impaired renal or hepatic function.
  • hypertension treated with α methyldopa, clonidine, or beta-adrenergic blockers.
  • if they have used opioid analgesics within the previous 24 hr.
  • previous sensitivity to local anesthetics.

研究组 & 干预措施

Group A (control group)

Active Comparator

Patients in each received 10 ml 0.5 % bupivacaine and 1µg/kg dexmedetomidine diluted in 10 ml saline injected intra-articularly without lidocaine patch

干预措施: Dexmedetomidine Bupivacaine (Drug)

Group B

Experimental

Patients in each received 10 ml 0.5 % bupivacaine and 1µg/kg dexmedetomidine diluted in 10 ml saline injected intra-articularly with a patch of lidocaine 5% was applied to the skin

干预措施: Lidocaine 5% patch with Dexmedetomidine Bupivacaine (Drug)

结局指标

主要结局

The total dose of postoperative pethidine consumption

时间窗: 24 hours

The total dose of postoperative pethidine consumption; Pethidine 20 mg was given as rescue analgesia if pain visual analogue visual analogue scale (VAS) ≥4.

次要结局

  • First postoperative analgesia request time(24 hours)
  • Pain intensity(24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ahmed Said Elgebaly,MD

Assistant professor of Anesthesiology, Surgical Intensive Care

Tanta University

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