Health Trials

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

ConditionHip Fracture Surgeries
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorAin Shams University

About this trial

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 criteria

Qualifiers

Age 18-70 years.

ASA I-II.

Confirmed primary unilateral hip fracture.

Scheduled for surgery under spinal anesthesia.

Disqualifiers

Allergy to local anesthetics.

Coagulopathy or on anticoagulant therapy.

Infection at injection site.

Pre-existing neurological deficits in the lower limbs.

Trial design

Treatments tested in this trial

  • PENG Block
  • LCFN block
  • bupivacaine 0.25%.
  • Xylocaine 2 %

Treatment groups

24 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Ain Shams University

Lead sponsor

Source ClinicalTrials.gov