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Ultrasound-Guided PENG Block vs Femoral Nerve Block for Analgesia Before Spinal Anesthesia in Hip Fracture Surgery

Comparative Study of Preoperative Ultrasound-Guided Pericapsular Nerve Group Block and Femoral Nerve Block for Analgesia Before Spinal Anesthesia in Proximal Femur Fracture Fixation

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06989047
Enrollment
60
Registered
2025-05-25
Start date
2025-05-30
Completion date
2026-05-30
Last updated
2025-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fracture, Pain Management, Proximal Femur Fracture, Spinal Anesthesia

Keywords

Pericapsular Nerve Group Block (PENG), Femoral Nerve Block (FNB), Ultrasound-Guided Nerve Block, Spinal Anesthesia, Hip Surgery, Regional Anesthesia

Brief summary

This study will compare two types of ultrasound-guided nerve blocks-Pericapsular Nerve Group (PENG) block and Femoral Nerve Block (FNB)-to evaluate their effectiveness in reducing pain before spinal anesthesia in patients who will undergo surgery for proximal femur fractures. Proximal femur fractures will continue to be common, especially in older adults, and often will cause severe pain that will make it difficult to position patients for spinal anesthesia. Both nerve blocks will aim to reduce pain, improve comfort during spinal anesthesia, and decrease the need for postoperative pain medication. A total of 60 adult patients who will undergo proximal femur fracture fixation under spinal anesthesia will be enrolled and randomly assigned to receive either a Pericapsular Nerve Group (PENG) block or a femoral nerve block before the procedure. The study will monitor patients' pain scores using the Visual Analog Scale (VAS) at multiple time points, including during positioning and throughout the first 24 hours after surgery. It also will evaluate how long it will take before the patients require rescue pain medication, and how much total pain medication will be needed.

Interventions

PROCEDUREPericapsular Nerve Group (PENG) Block

Assigned Interventions: Procedure/Surgery: Pericapsular Nerve Group (PENG) Block An ultrasound-guided nerve block targeting articular branches of the femoral, obturator, and accessory obturator nerves. Performed under aseptic technique using a curved low-frequency ultrasound probe to visualize the iliopsoas plane and pubic ramus. Drug: Bupivacaine (0.25%, 30 ml) Local anesthetic used to provide analgesia in nerve block. Drug: Magnesium sulfate (10%, 5 ml = 500 mg) Adjunct used to enhance analgesic efficacy of the block.

An ultrasound-guided nerve block targeting the femoral nerve to provide analgesia before spinal anesthesia in proximal femur fracture surgery. Administered using 30 ml of 0.25% bupivacaine and 5 ml of 10% magnesium sulfate (500 mg). The block is performed with an in-plane ultrasound approach, identifying the femoral nerve lateral to the femoral artery under sterile conditions.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Scheduled for proximal femur fracture fixation under spinal anesthesia * Classified as American Society of Anesthesiologists (ASA) physical status I, II, or III * Ability to understand and use the Visual Analog Scale (VAS) * Provided written informed consent

Exclusion criteria

* Coagulopathy * Local infection at the injection site * Known allergy to local anesthetics or magnesium sulfate * Severe cardiopulmonary disease \[American Society of Anesthesiologists (ASA) ≥ IV\] * Preexisting diabetic or other neuropathies * Chronic opioid use * Contraindication to spinal anesthesia * Cognitive impairment or inability to comprehend Visual Analog Scale (VAS)

Design outcomes

Primary

MeasureTime frameDescription
Time to First Rescue AnalgesiaWithin 24 hours postoperativelyThe time (in hours) from the end of the nerve block to the first request for additional analgesia (nalbuphine 0.2 mg/kg IV) will be recorded for each patient.
Pain Score During Positioning for Spinal Anesthesia Using Visual Analog Scale (VAS)Immediately before spinal anesthesia (within 15 minutes post-block)The Visual Analog Scale (VAS) will be used to assess pain intensity during positioning for spinal anesthesia. The VAS is a 10 cm line where 0 indicates no pain and 10 indicates the worst imaginable pain. The score will be recorded immediately before spinal anesthesia after performing either the PENG block or femoral nerve block.

Secondary

MeasureTime frameDescription
Total Nalbuphine Consumption24 hours postoperativelyThe cumulative dose (in mg) of intravenous nalbuphine administered for pain control will be calculated for each participant over the first 24 hours following surgery.
Mean Arterial Pressure (MAP) ChangesFrom baseline up to 24 hours postoperativelyMean arterial pressure will be recorded at baseline (pre-block), then at 2, 5, 10, 15 minutes post-block, and subsequently at 2, 6, 12, 18, and 24 hours after surgery to evaluate hemodynamic stability following either pericapsular nerve block (PENG) block or femoral nerve block.
Patient Satisfaction ScoreAt 24 hours postoperativelyPatient satisfaction with pain control will be evaluated using a 5-point Likert scale (1 = very dissatisfied, 5 = very satisfied) at the end of the 24-hour postoperative period.

Contacts

Primary ContactMohamed K Ammar, M.B.B.Ch
Mohamed_Khaled@med.asu.edu.eg01153702277

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026