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Analgesic Comparison of PENG/LFCN to FICB for Total Hip Arthroplasty — PengvsFICB  

Analgesia Clinical Trial

Official title:
Analgesic Comparison of Pericapsular Nerve Group (PENG) Block and Lateral Femoral Cutaneous Nerve (LFCN) Block to Fascia Iliaca Compartment Block (FICB) in Patients Undergoing Primary Total Hip Arthroplasty (THA).

Clinical Trial Summary

This study compares 2 commonly used interventions (regional pain blocks) used in hip arthroplasty for pain control. One of the interventions is newer and not widely established.

Clinical Trial Description

This study will compare the FICB to the PENG/LFCN blocks. Patient reported pain scores on a verbal numeric rating scale will be utilized and recorded in the PACU and postoperatively at 3, 6, 12, 18, 24, 36 and 48 hours after patient arrival in the PACU. Additionally, opioid consumption will be converted to morphine milliequivalents and compared between groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05477641
Study type Interventional
Source SSM Health Bone and Joint Hospital at St Anthony
Contact
Status Recruiting
Phase N/A
Start date July 28, 2022
Completion date February 1, 2023
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