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

Not Applicable

Recruiting

• Conditions: Hip Fractures
• Interventions: Procedure: pericapsular nerve group (PENG) block

• Registration Number: NCT05941221
• Lead Sponsor: Ain Shams University

Brief Summary

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 .

Detailed Description

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%.

Study Timeline

• Study Start: 2023-03-30
• Study First Submitted: 2023-06-24
• Status Verified: 2023-07
• Study First Submitted QC: 2023-07-03
• Last Update Submitted: 2023-07-03
• Study First Posted: 2023-07-12
• Last Update Posted: 2023-07-12
• Primary Completion: 2023-08
• Study Completion: 2023-09

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 16

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
study group	pericapsular nerve group (PENG) block	patients will receive pericapsular nerve group (PENG )block through ultrasound at the end of the surgery.

Primary Outcome Measures

Name	Time	Method
post operative analgesic effect of PENG block	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

Secondary Outcome Measures

Name	Time	Method
post operative complications	24 hours	evaluate the effect of PENG block in reducing post operative complications like incidence of delirium using RAMSAY score

Trial Locations

Locations (1)

Ain Shams University Hospital; 🇪🇬 Cairo, Egypt