PENG Block for Total Hip Arthroplasty

Status Completed

Clinical Trial Summary

This randomized, double-blinded, placebo-controlled trial seeks to evaluate the efficacy of the pericapsular nerve group block on postoperative rehabilitation.

Clinical Trial Description

The pericapsular nerve group, or PENG block, has been recently described and shows promise in providing analgesia to the hip joint. However, the effect of this block on postoperative rehabilitation is uncertain. This study compares a preoperative PENG block to a placebo before total hip arthroplasty under spinal anesthesia. The primary outcome measure is verticalization, walking distance, ability to go out of bed, active lifting of the limb, range of motion in the hip joint, bending range of motion, and abduction range of motion. The secondary measure is postoperative pain assessment during rehabilitation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05944380
Study type	Interventional
Source	Poznan University of Medical Sciences
Contact
Status	Completed
Phase	Phase 4
Start date	June 16, 2020
Completion date	January 30, 2023

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