Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07104097

Comparison Between 2 Techniques for Lumbar-ESPB

Led by Papa Giovanni XXIII Hospital · Updated on 2026-05-12

44

Participants Needed

1

Research Sites

45 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Comparison Between 2 Techniques for Lumbar-ESPB

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Primary total hip replacement surgery
  • Patient provides informed consent
Not Eligible

You will not qualify if you...

  • Allergies to any study drugs
  • Contraindications to spinal anesthesia
  • Kidney failure with GFR less than 30
  • Epilepsy, psychiatric diseases, or neurological deficits
  • Revision hip surgery
  • Neuropathies in the lumbar area such as tingling, numbness, or motor deficits
  • Lack of informed consent
  • Pregnancy
  • Alcohol or opioid abuse
  • Emergency surgery or intensive care admission

AI-Screening

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Trial Site Locations

Total: 1 location

1

Aast Papa Giovanni Xxiii

Bergamo, Italy, 24127

Actively Recruiting

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Research Team

D

Dario Bugada

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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