Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT07240961

Lumbal Erector Spinae Plane Block for Pain Management After Total Hip Arthroplasty

Led by University Tunis El Manar · Updated on 2025-11-21

60

Participants Needed

1

Research Sites

35 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The Erector Spinae Plane (ESP) block or spinal erector block was first described in September 2016 by a Canadian team. It's a block that was initially used for the treatment of chronic thoracic neuropathic pain. The ESP block is one of the inter-fascicular blocks and it's an easy-to-perform technique.In the literature, it has been reported that Lumbar ESPB provides effective analgesia after a hip surgery. The purpose of this prospective randomized study was to compare the analgesic effects of the ultrasound-guided lumbar Erector Spinae Plane block on postoperative pain management versus the multimodal analgesia after total hip arthroplasty.

CONDITIONS

Official Title

Lumbal Erector Spinae Plane Block for Pain Management After Total Hip Arthroplasty

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults undergoing primary total hip arthroplasty with a lateral approach under general anesthesia
Not Eligible

You will not qualify if you...

  • Contraindication or refusal of regional anesthesia
  • Contraindication to non-steroidal anti-inflammatory drugs (NSAIDs)
  • Allergy to opioids
  • Allergy to paracetamol
  • Creatinine clearance less than 30 ml/min
  • Weight less than 50 kg or greater than 100 kg
  • Psychiatric disorders or difficulty communicating
  • Presence of lower limb neurological deficit
  • Undergoing bilateral or revision total hip replacement

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kassab Orthopedic Institute

Manouba, Tunisia, 2010

Actively Recruiting

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Research Team

K

KAABACHI OLFA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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