RecruitingNot ApplicableNCT07687290

Comparative Study Between Pericapsular Nerve Group Block (PENG) And Pericapsular Nerve Group (PENG) Block Combined With Lateral Femoral Cutaneous Nerve (LFCN) Block for Positioning Analgesia Prior to Spinal Anesthesia in Hip Fracture Patients


Sponsor

Ain Shams University

Enrollment

24 participants

Start Date

Jun 18, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

To evaluate and compare the effectiveness of the Pericapsular Nerve Group (PENG) block alone versus the PENG block combined with the Lateral Femoral Cutaneous Nerve (LFCN) block in providing adequate analgesia for patient positioning during spinal anesthesia in individuals undergoing surgery for hip fracture.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called LCFN block, a procedure called PENG Block, and others for people with hip fracture surgeries. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 70 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREPENG Block

Pericapsular Nerve Group Block

PROCEDURELCFN block

Lateral Femoral Cutaneous Nerve block

DRUGbupivacaine 0.25%.

0.25% of Bupivacaine (Bupivacaine 0.5% is added to Lidocaine 2% in the same volume)

DRUGXylocaine 2 %

local infilteration at the insertion site


Locations(1)

Ain Shams University

Cairo, Egypt

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NCT07687290


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