Total Knee Replacement With Tourniquet or Aquamantys

Status Completed

Clinical Trial Summary

The purpose of this study is to compare quadriceps muscle strength, pain, opioid consumption and patient function during the first three months after short-stay total knee replacement between patients treated with short-duration tourniquet knee replacement with the Aquamantys® bipolar sealer versus those treated with the standard of care (tourniquet used throughout the case and no Aquamantys®). By doing this study, investigators hope to learn if short duration tourniquet knee replacement with the Aquamantys® bipolar sealer is more effective than standard of care (tourniquet used throughout the case and no Aquamantys®). The purpose of this study is to compare quadriceps muscle strength, pain, opioid consumption and patient function during the first three months after short-stay total knee replacement between patients treated with short-duration tourniquet knee replacement with the Aquamantys® bipolar sealer versus those treated with the standard of care (tourniquet used throughout the case and no Aquamantys®).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Knee Replacement

Clinical Trial Details

NCT number	NCT04016285
Study type	Interventional
Source	University of Kentucky
Contact
Status	Completed
Phase	N/A
Start date	January 15, 2019
Completion date	April 18, 2023

View Details

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