Adductor Canal Block for Medial Compartment Knee Arthroplasty

Status Completed

Clinical Trial Summary

This study will evaluate the affects of a single injection ultrasound-guided adductor canal block for patients undergoing robotic-assisted (MAKOplasty) medial UKA (unicompartmental knee arthroplasty). Specifically, this study will compare the adequacy of postoperative analgesia provided by the adductor canal block with that provided by single injection lumbar plexus blockade. The working hypothesis is that the analgesia provided by the adductor canal block will be equivalent to the analgesia provided by the lumbar plexus block. The primary outcome will be a comparison of verbal numerical pain scores at rest and with movement over the first 24 hours following nerve blockade.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Medial Unicompartmental Knee Arthroplasty
Postoperative Analgesia

Clinical Trial Details

NCT number	NCT01818531
Study type	Interventional
Source	Wake Forest University Health Sciences
Contact
Status	Completed
Phase	Phase 4
Start date	April 2013
Completion date	May 2015

View Details

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