Clinical Trials Directory

Trials / Completed

CompletedNCT06083428

Erector Spinae vs. PENG Block for Total Hip Arthroplasty

Erector Spinae Plane Block (ESPB) vs. PENG Block for Pain Management and Stress Response in Patients Undergoing Total Hip Arthroplasty. A Prospective, Randomized Trial.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Poznan University of Medical Sciences · Academic / Other
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Effect of PENG block and ESPB on pain management, and NLR and PLR following knee arthroplasty

Detailed description

Hip arthroplasty is one of the most common orthopedic procedures, especially in elderly patients, due to the deformation of joints. Patients may complain of severe pain due to surgical trauma and prosthesis. Regional anesthesia methods may be performed to reduce the inflammatory response, opioid consumption, and opioid-related side effects. In recent years, the influence of regional anesthesiology on reducing the inflammatory response after surgical procedures has been emphasized. However, very few studies have evaluated the effect of various methods of anesthesia on the NLR. This is the first study to investigate the effect of regional anesthesia on the NLR and PLR in patients undergoing hip replacement surgery.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine 0.2% Injectable Solution Erector Spinae Plane Blockultrasound guided ESPB - L4 level, unilateral
DRUGRopivacaine 0.2% Injectable Solution - PENG blockultrasound guided PENG block
DRUGControl TestOnly spinal anesthesia

Timeline

Start date
2023-10-17
Primary completion
2024-06-11
Completion
2024-06-11
First posted
2023-10-16
Last updated
2024-06-18

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT06083428. Inclusion in this directory is not an endorsement.