IPACK Block in Total Knee Arthroplasty

Status Recruiting

Clinical Trial Summary

100 patients ASA I-III, undergoing total knee arthroplasty under spinal anesthesia, will be randomly assigned into one of two groups, namely group A (n=50), where an adductor canal block and an IPACK block will be performed preoperatively and group B (n=50) where an adductor canal block only will be performed preoperatively. All patients will receive a standardized multimodal approach, including pregabalin, paracetamol, and PCA with morphine. NRS scores in static and dynamic conditions during the first 48 hours postoperatively, morphine consumption during the first 24 hours postoperatively will be measured and additionally, patient satisfaction, complications, range of knee motion, moblization, functionality, delirium ocurence will be recorded. Chronic pain will be assessed in 3 and 6 months postoperatively.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Total Knee Arthroplasty

Clinical Trial Details

NCT number	NCT03692858
Study type	Interventional
Source	Asklepieion Voulas General Hospital
Contact	Alexandros Makris
Phone	+306947076446
Email	makrisalexandros@hotmail.com
Status	Recruiting
Phase	Phase 2
Start date	October 1, 2018
Completion date	July 2020

View Details

See also
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