Actively Recruiting
Sacral Erector Spinae Plane Block Versus Pericapsular Nerve Group Block For Analgesia In Hip Hemiarthroplasty A Randomized Comparative Study
Led by Fayoum University Hospital · Updated on 2026-03-03
80
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare two types of nerve blocks, sacral erector spinae plane block S-ESPB and pericapsular nerve group PENG block, for pain relief after hip hemiarthroplasty in patients aged 50 to 90 years with femoral neck fractures. These blocks are being studied because they may provide effective pain control while preserving muscle strength, aligning with recovery protocols that emphasize pain management, limited opioid use, and early movement to reduce complications. Participants will be randomly assigned to receive either the sacral ESPB or the PENG block after spinal anesthesia and before surgery begins. The sacral ESPB is performed with the patient lying on their side, while the PENG block is done with the patient lying on their back. Both blocks use ultrasound guidance to accurately place local anesthetic near targeted nerves, with strict safety measures to avoid toxicity and adverse events. All patients will receive standard spinal anesthesia and a uniform pain medication plan including paracetamol, NSAIDs, and opioids if needed. During the study, patients will be monitored for pain levels using a numeric rating scale at rest and during movement at multiple times within 24 hours after surgery. Other measures include opioid use, timing of first rescue pain medication, ability to participate in physiotherapy, delirium signs, motor function, side effects linked to opioids, and hospital stay length. Safety monitoring will check for block-related complications and adverse reactions. Total participation covers the surgery day and up to 30 days of follow-up for hospital discharge assessment.
CONDITIONS
Brief Title
Sacral ESPB vs. PENG Block for Hip Hemiarthroplasty Analgesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 50 to 90 years of any gender
- Diagnosed with intracapsular neck of femur fracture scheduled for elective hip hemiarthroplasty
- American Society of Anesthesiologists (ASA) physical status I to III
You will not qualify if you...
- Patient refusal to participate
- Allergy to local anesthetics or infection at the injection site of the block
- Contraindication to spinal anesthesia
- Blood clotting disorders (INR ≥ 1.5 or platelets ≤ 80 × 10^3/microliter)
- Body mass index greater than 35 kg/m2
- Peripheral neuropathy or diabetic neuropathy
- Receiving opioids for chronic pain therapy
- Cognitive impairment preventing pain scoring
- Chronic renal failure requiring dose modification
- Bilateral hip fracture or previous surgery on the same hip
Research Team
S
Samar Ahmed Ramadan
M
Mohamed Ahmed Hamed
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