跳至主要内容
临床试验/NCT05941221
NCT05941221招募中不适用

Effect of Pericapsular Nerve Group (PENG) Block for Perioperative Analgesia in Geriatric Patients With Hip Fractures

Ain Shams University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2023年3月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
16
试验地点
1
主要终点
post operative analgesic effect of PENG block

研究概览

简要总结

the goal of this clinical trial is to evaluate the analgesic effect of pericapsular nerve group (PENG) block in elderly patients with hip fractures undergoing hip surgery .

and to evaluate its effect in reducing post operative complications .

详细描述

all patients meeting the inclusion criteria will be informed about the study goal , methods and procedure in clear language. a written informed consent will be taken.

All patients ,once arrived to the OR, monitor will be attached, spinal anesthesia will be performed as follows, after sterilization of the back with bovidon iodine, local anesthesia 3cc of lidocaine 20% will be injected at the level of L3-L4 spine , then injection of 17 mg bupivacaine 0.5% through a 25 spinal needle.

At the end of surgery,all patients will receive PENG block through ultrasound. The regional block was performed with the patient in the supine position. A curvilinear low-frequency ultrasound probe (2-5MHz) was initially placed in a transverse plane over the AIIS and then aligned with the pubic ramus by rotating the probe counterclockwise approximately 45 degrees. In this view, the IPE, the iliopsoas muscle and tendon, the femoral artery, and pectineus muscle were observed. A 22-gauge, 80-mm needle was inserted from lateral to medial in an in-plane approach to place the tip in the musculofascial plane between the psoas tendon anteriorly and the pubic ramus posteriorly. Following negative aspiration, the local anesthetic solution was injected in 5-mL increments while observing for adequate fluid spread in this plane for a total volume of 20 mL bupivacaine 0.25%.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
60 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients must age 60 years or more .
  • patients must belong to american society of anesthesiologists (ASA) classification class II or III

排除标准

  • age < 60 years
  • refusal of peripheral nerve block
  • infection at the site of injection
  • coagulopathy INR > 1.8
  • platelets count < 50,000
  • known allergy to used medications.

结局指标

主要结局

post operative analgesic effect of PENG block

时间窗: 24 hours

evaluate the analgesic effect of PENG block in the post operative period both at rest and with movement using the Visual analog scale for pain

次要结局

  • post operative complications(24 hours)

研究者

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

Lydia edward aziz zakhary

Principal Investigator

Ain Shams University

研究点 (1)

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