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临床试验/NCT07838480
NCT07838480已完成不适用

Ultrasound Guided Femoral Nerve Block Versus Adductor Canal Block by Using Bupivacaine and Magnesium Sulphate for Post-Operative Analgesia After Knee Arthroscopic Surgeries

Tanta University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年11月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
90
试验地点
1
主要终点
The total post-operative morphine consumption

研究概览

简要总结

Ultrasound Guided Femoral Nerve Block versus Adductor Canal Block by Using Bupivacaine and Magnesium Sulphate

详细描述

Ultrasound Guided Femoral Nerve Block versus Adductor Canal Block by Using Bupivacaine and Magnesium Sulphate for Post-Operative Analgesia after knee Arthroscopic Surgeries: A Randomized Controlled Study

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • •Age 21-60 years,
  • •both sexes, American Society of Anesthesiologists classification I-II and - -patients scheduled for elective Knee arthroscopic surgeries under spinal anesthesia.

排除标准

  • •Patient refusal.
  • •Patients on chronic pain medications or have a history of substance abuse.
  • •Patients who are unable to describe their postoperative pain (neuropsychiatric disorder).
  • •Patients with a history of coagulopathy.
  • •Patient with morbid obesity (body mass index ≥40 kg/m2).
  • •Patients with known local anesthetics and opioid allergy.
  • •Patients with infection at the site of the needle puncture.
  • •Patients with major respiratory, cardiac, renal or hepatic disorders.
  • •Patients on calcium channel blockers.

研究组 & 干预措施

Group I: control group

Placebo Comparator

Group I: 30 Patients will receive the standard spinal anesthesia 12.5 mg (2.5 ml) of 0.5% hyperbaric bupivacaine with 25 µg of fentanyl (0.5 ml), with no intervention as a control group.

干预措施: Group I: control group (Procedure)

Group II: Ultrasound Guided Femoral Nerve Block

Experimental

Group II: 30 Patients will receive the standard spinal anesthesia 12.5 mg (2.5 ml) of 0.5% hyperbaric bupivacaine with 25 µg of fentanyl (0.5 ml), then US guided FNB will be performed at the end of surgery, with 20 ml of 0.25% bupivacaine with 5 ml of magnesium sulfate 10% solution (500 mg) with total volume of 25 ml.

干预措施: Group II: Ultrasound Guided Femoral Nerve Block (Procedure)

Group III : Adductor Canal Block group

Experimental

Group III: 30 Patients will receive the standard spinal anesthesia 12.5 mg (2.5 ml) of 0.5% hyperbaric bupivacaine with 25 µg of fentanyl (0.5 ml), then US guided ACB will be performed at the end of surgery, with 20 ml 0.25% bupivacaine with 5 ml of magnesium sulfate 10% solution (500 mg) with total volume of 25 ml.

干预措施: group III : Adductor Canal Block group (Procedure)

结局指标

主要结局

The total post-operative morphine consumption

时间窗: 24 hours postoperatively

次要结局

  • Assessment of pain by Numeric Rating Scale(Immediately after discharge to the PACU and ward at 1hour, 3hour, 6hour, 12hour, 24 hours.)

研究者

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

Nourhan Aladdin Ali Khidr

Resident of Anesthesia, Surgical Intensive Care and Pain Management

Tanta University

研究点 (1)

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