Actively Recruiting

Phase Not Applicable
Age: 50Years - 90Years
All Genders
ID07442721

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

Age: 50Years - 90Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Day of surgery

Participants receive spinal anesthesia followed by either a sacral erector spinae plane block or a PENG block before surgery to manage pain during hip hemiarthroplasty.

1 visit (in-person, on surgery day)

Post-operative Follow-up

Duration - Up to 30 days post-surgery

Participants are monitored for pain, opioid consumption, motor block, side effects, and adverse events during the first 24 hours after surgery, with delirium assessments twice daily for 3 days and hospital stay up to 30 days.

Multiple visits for up to 30 days including assessments at 2, 4, 6, 8, 12, 18, 24 hours postoperatively and twice daily delirium assessments for 3 days

Trial Site Locations

Total: 1 location

1

Fayoum University hospita

El Fayoum Qesm, Faiyum Governorate, Egypt, 63514

Actively Recruiting

Loading map...

Research Team

S

Samar Ahmed Ramadan

M

Mohamed Ahmed Hamed

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Similar Trials

A Clinical Follow-up Study on the Efficacy of Thumbtack Need...

Postoperative Complications

Actively Recruiting

2 locations

Continuous Post-operative Lidocaine Infusion Following Major...

Postoperative Delirium

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

Perioperative utilization of tranexamic acid in total knee and hip arthroplasty procedures in Poland - a survey-based study.

Dorota Studzińska, Izabela Pabjańczyk, Kamil Polok...

https://pubmed.ncbi.nlm.nih.gov/39451168

The use of the ERAS protocol in malnourished and properly nourished patients undergoing elective surgery: a questionnaire study.

Paweł Kutnik, Michał Bierut, Elżbieta Rypulak...

https://pubmed.ncbi.nlm.nih.gov/38282499

Pain management after total knee arthroplasty: PROcedure SPEcific Postoperative Pain ManagemenT recommendations.

Patricia M Lavand'homme, Henrik Kehlet, Narinder Rawal...

https://pubmed.ncbi.nlm.nih.gov/35852550

Randomized comparison between pericapsular nerve group (PENG) block and suprainguinal fascia iliaca block for total hip arthroplasty.

Julián Aliste, Sebastián Layera, Daniela Bravo...

https://pubmed.ncbi.nlm.nih.gov/34290085

Comparison of Pericapsular Nerve Group Block versus Fascia Iliaca Compartment Block as Postoperative Pain Management in Hip Fracture Surgeries.

K S Senthil, Prem Kumar, Lakshmi Ramakrishnan

https://pubmed.ncbi.nlm.nih.gov/35422548