Low-Volume PENG Block With Dexamethasone After Hip Replacement
Official title: Low-Volume PENG Block With Dexamethasone Versus Standard-Volume PENG Block for Postoperative Analgesia and Quadriceps Function After Total Hip Arthroplasty
Run by Ain Shams University · NCT07855341 · Data updated 2026-11-12
This trial tests whether a smaller PENG block with dexamethasone provides similar pain relief but preserves quadriceps strength after hip replacement, compared with the standard-volume PENG block.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 50 Years to 70 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo, Cairo Governorate) |
| Status | Recruiting |
| Started | October 15, 2026 |
| Main results expected | August 31, 2027 |
| Study ends | September 14, 2027 |
| Registry record updated | October 16, 2026 |
| Trial ID | NCT07855341 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 50-70 undergoing elective primary unilateral total hip arthroplasty under spinal anesthesia who are ASA I or II.
✕Probably not a fit
Patients who do not respond to dexamethasone optimization or who experience longer analgesic duration with low-volume blocks may see limited benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional phase 4 study compares two ultrasound-guided PENG block regimens in adults undergoing primary unilateral total hip arthroplasty under spinal anesthesia. The low-volume approach uses 10 mL of bupivacaine 0.25% with 4 mg dexamethasone, aiming to reduce spread to the femoral nerve and preserve quadriceps function, while potentially shortening analgesic duration. The standard-volume approach uses 20 mL of bupivacaine 0.25% without specified corticosteroid optimization beyond multimodal analgesia. Outcomes focus on time to first rescue analgesia and postoperative pain and mobility, with attention to opioid-sparing effects and motor preservation. Background context notes that PENG blocks target articular branches around the hip and have shown analgesic benefits, but motor-sparing claims with higher volumes may not always hold.
Why it matters
Potential benefit: If successful, patients may experience effective pain control with better quadriceps strength, enabling earlier mobilization after hip replacement.
How similar studies have gone: Previous analyses and meta-analyses suggest PENG blocks reduce opioid needs and pain, but the impact of low-volume, dexamethasone-augmented regimens requires confirmation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Physical status ASA I or II. * Age 50-70 years. * Patients scheduled for elective primary unilateral total hip arthroplasty under spinal anaesthesia. * No sex predilection. Exclusion Criteria: * Patient refusal. * Physical status ASA III or above. * Contraindications to spinal anaesthesia (coagulopathy, local infection at injection site, raised intracranial pressure). * Revision or bilateral total hip arthroplasty. * Known allergy or hypersensitivity to study drugs (bupivacaine, dexamethasone) or to any component of the multimodal analgesic regimen (paracetamol, nalbuphine). * Pre-existing neuromuscular disease, lower-limb motor deficit, or neuropathic pain syndrome. * Uncontrolled diabetes mellitus (HbA1c \> 8% or fasting blood glucose \> 180 mg/dL) or any contraindication to corticosteroids. * Cognitive impairment precluding pain and motor assessment, or chronic opioid use. * Body mass index greater than 40 kg/m2 precluding adequate ultrasound visualization.
Where it's running
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Ain Shams University Hospitals (El Demerdash Hospital)
Cairo, Cairo Governorate, Egypt Recruiting
Study contacts
- Principal investigator: Mohamed F Morsi, M.B., B.Ch., M.Sc. — Faculty of Medicine, Ain Shams University
- Study coordinator: Mohamed F Morsi, M.B., B.Ch., M.Sc.
- Email: MohamedMorsi@med.asu.edu.eg
- Phone: +201116618163
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.