PENG Block vs Intrathecal Morphine in Total Hip Arthroplasty

Status Completed

Clinical Trial Summary

To compare the impact of pericapsular nerve group (PENG) block to intrathecal morphine on postoperative analgesia, motor function and side effects in patients undergoing primary total hip arthroplasty under spinal anesthesia.

Clinical Trial Description

The study aims to confirm the non-inferiority of PENG block vs intrathecal morphine in patients undergoing total hip arthroplasty under spinal anesthesia. Non-inferiority will be assessed regarding maximum pain on a numerical rating scale at rest and during active hip flexion and regarding cumulative morphine consumption during 48 postoperative hours. Impact on quadriceps muscle motor function and side effects including pruritus, nausea and vomiting and hypotension will also be assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05308420
Study type	Interventional
Source	Akromion Special Hospital for Orthopedic Surgery
Contact
Status	Completed
Phase	Phase 4
Start date	April 3, 2022
Completion date	December 1, 2022

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