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Search / Trial NCT06964282

Iliopsoas (IPB) and Pericapsular Nerve Group (PENG) Blocks Comparison on Analgesia and Recovery After Total Hip Arthroplasty

Launched by UNIVERSITY OF LIEGE · Apr 30, 2025

Trial Information

Current as of July 26, 2025

Not yet recruiting

Keywords

ClinConnect Summary

This clinical trial is comparing two pain relief techniques, called the iliopsoas plane block (IPB) and the PENG block, for patients undergoing total hip replacement surgery. Both methods use a local anesthetic to help manage pain after surgery, but this study aims to see if they work equally well. A total of 118 adult patients who are scheduled for hip replacement will be randomly assigned to receive one of these two blocks before their surgery, and their pain levels will be monitored for 48 hours afterward.

To be eligible for this trial, participants must be adults over 18 years old, scheduled for hip replacement surgery, and have a general health status that is stable. People with certain conditions, such as pregnancy, chronic pain issues, or serious allergies to local anesthetics, will not be included. Participants can expect to receive standard pain relief after their surgery, and their recovery will be assessed through various measures, including how much pain they feel, how well they can walk, and their overall satisfaction with the recovery process. This study is important because if the IPB is found to be as effective as the PENG block, it could give doctors more options for managing pain and helping patients recover after hip surgery.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Adult patients (age \>18 years) ASA physical status classification I-III Scheduled for elective posterior approach total hip arthroplasty (THA) under spinal anesthesia
  • Exclusion Criteria:
  • Pregnancy (confirmed by beta-HCG test if applicable) Known peripheral neuropathy or major neurological disease Chronic pain syndromes or long-term opioid use (\>20 mg oral morphine equivalents/day) Severe hepatic or renal insufficiency Allergy to local anesthetics Major coagulopathies Vulnerable patients (e.g., minors, legally protected individuals)

About University Of Liege

The University of Liège, a prestigious research institution in Belgium, is committed to advancing medical science through innovative clinical trials. With a focus on interdisciplinary collaboration, the university leverages its extensive expertise in various fields, including medicine, pharmacology, and biomedical engineering, to conduct high-quality research aimed at improving patient outcomes. The institution fosters a rigorous ethical framework and adheres to international standards in clinical research, ensuring the integrity and reliability of its studies. Through its clinical trials, the University of Liège aims to contribute significantly to the development of novel therapeutic approaches and enhance the understanding of complex health issues.

Locations

Liège, , Belgium

Patients applied

0 patients applied

Trial Officials

Michele Carella, MD, PhD, ESRA-DRA

Principal Investigator

Liège University Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported