iPACK Block for Total Knee Arthroplasty

Status Active, not recruiting

Clinical Trial Summary

This randomized, double-blinded, placebo-controlled trial seeks to evaluate the efficacy of the rehabilitation process of the Interspace between the Popliteal Artery and Capsule of the Posterior Knee (iPACK) block in total knee arthroplasty.

Clinical Trial Description

The Interspace between the Popliteal Artery and Capsule of the Posterior Knee (iPACK) block, has been recently described and shows promise in providing analgesia to the knee joint. The effect of this block on postoperative rehabilitation is uncertain. This study aims to compare a preoperative iPACK block to a placebo block prior to total knee 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	NCT06087562
Study type	Interventional
Source	Poznan University of Medical Sciences
Contact
Status	Active, not recruiting
Phase	Phase 4
Start date	June 16, 2020
Completion date	December 30, 2024

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