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临床试验/NCT05833776
NCT05833776已完成不适用

Value of IPACK Block (Interspace Between the Popliteal Artery and Capsule of Knee) With Spinal Anesthesia Versus Fentanyl Based Spinal Anesthesia on Postoperative Analgesia for Knee Arthroscopic Meniscectomy

Azhar University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年1月1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
发起方
入组人数
60
试验地点
1
主要终点
post-operative analgesia

研究概览

简要总结

Postoperative analgesia is provided by local anesthesia combined with intrathecal narcotics. In addition, for the first 24 hours, this combination has a parenteral opioid sparing effect. However, despite its benefits, this method has been associated to an increased incidence of urine retention, nausea, and vomiting, as well as pruritus. A new localized analgesic approach called as IPACK (infiltration between the knee capsule and the popliteal artery) has been employed in practice.

详细描述

The goal of this study was to compare fentanyl based spinal anesthesia to IPACK Block-based spinal anesthesia during knee arthroscopy.

Patients and Methods: The study enrolled sixty patients with ASA (I-II) ranging in age from 25 to 60 years old after receiving ethical committee permission and written informed consent from patients. They were divided into two groups: group F (30 patients) received spinal anesthesia using hyperbaric bupivacaine 0.5% (3ml) with fentanyl (25ug) and group I (30 patients) received spinal anesthesia using hyperbaric bupivacaine 0.5% (3ml) with IPACK Block using plain bupivacaine 0.5% (15ml). Results: In the first 4 hours postoperatively, there were no variations in VAS scores between the two groups; however, following 4 hours and over the next 12 hours, Group I, VAS scores were lower. The amount of morphine used overall was lower in Group I, which took longer than Group F to reach initial rescue analgesia. The level of patient satisfaction 48 hours after surgery was higher in group I than in group F.

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
Single (Participant)

入排标准

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

入选标准

  • •age from 25 to 60 years old, with ASA physical status I-III undergoing for knee arthroscopy

排除标准

  • •Patient refusal, neuromuscular diseases, allergies to local anesthetics, and contraindications to spinal anesthesia such as coagulopathy and severe mitral stenosis

研究组 & 干预措施

group F

Experimental

received spinal anesthesia using hyperbaric bupivacaine 0.5% (3ml) with fentanyl (25ug)

干预措施: spinal anesthesia using hyperbaric bupivacaine 0.5% (3ml) with fentanyl (25ug) (Procedure)

group I

Experimental

group I (30 patients) received spinal anesthesia using hyperbaric bupivacaine 0.5% (3ml) with IPACK Block using plain bupivacaine 0.5% (15ml).

干预措施: spinal anesthesia using hyperbaric bupivacaine 0.5% (3ml) with fentanyl (25ug) (Procedure)

结局指标

主要结局

post-operative analgesia

时间窗: 24 hours

post-operative pain relief

次要结局

未报告次要终点

研究者

发起方
Azhar University
申办方类型
Other
责任方
Principal Investigator
主要研究者

mohamed A Aboelsuod, MD

assistant professor of anesthesia intensive care and pain management

Al-Azhar University

研究点 (1)

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