Mepivacaine vs. Bupivacaine Spinal for TKA

Status Recruiting

Clinical Trial Summary

This study will enroll patients 18-75 years of age who are undergoing elective primary total knee replacement. The patients will be randomized to receive one of two spinal blocks: 1) mepivacaine or 2) bupivacaine. The primary goal is to determine which group arrives at recovery of motor function first. Ultimately, this study will explore if mepivacaine leads to earlier return of motor function and ultimately earlier movement and discharge times following total knee replacement.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Total Knee Replacement

Clinical Trial Details

NCT number	NCT05765682
Study type	Interventional
Source	Medical University of South Carolina
Contact	Haley Nitchie, MHA
Phone	843-792-1869
Email	nitchie@musc.edu
Status	Recruiting
Phase	N/A
Start date	March 13, 2023
Completion date	August 15, 2025

View Details

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