RecruitingNot ApplicableNCT07104097

Comparison Between 2 Techniques for Lumbar-ESPB

Regional Anesthesia in Hip Arthroplasty- Comparison Between Two Techniques for Erector Spinae Plane Block


Sponsor

Papa Giovanni XXIII Hospital

Enrollment

44 participants

Start Date

Oct 6, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Diffusion of local anesthetics after a lumbar ESPB within fascial planes towards nerve structures is a matter of debate. The main objective of the study is to compare the incidence of sensory block between two techniques of needle placement (superficial or translaminar) during lumbar ESPB block. Patients are treated with lumbar ESPB (randomized to superficial or translaminar), spinal anesthesia and multimodal analgesia. The primary endpoint will be the incidence of numbness/reduced skin sensitivity to cold (ice test) in the area innervated by the lumbar plexus. Secondary outcomes are pain and analgesic's consumption, motor block, quality of recovery and discharge ability.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Dexamethasone, a drug called Ibuprofen 400 mg, and others for people with hip surgery. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREspinal anesthesia

spinal anesthesia at L3-L4 plain bupivacaine 0.5% 2.2 ml

PROCEDUREsuperficial erector spinal plane block (ESPB)

Lidocaine 1% + ropivacaine 0.25% 30 ml with adrenaline 1:200.000 on top of L3 transverse process, between bone and erector spinae muscle

PROCEDUREdeep (inter laminar) erector spinal plane block (ESPB)

Lidocaine 1% + ropivacaine 0.25% 30 ml with adrenaline 1:200.000 between L3 and L4 transverse process, between erector spinae muscle and deep muscles

DRUGDexamethasone

8 mg iv preoperatively

DRUGIbuprofen 400 mg

preoperatively and postoperatively (every 8 hours)

DRUGParacetamol

1000 mg preoperatively and postoperatively (every 8 hours)

DRUGMorphine

Patient Controlled Analgesia


Locations(1)

Aast Papa Giovanni Xxiii

Bergamo, Italy

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NCT07104097


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