Clinical Trials Directory

Trials / Completed

CompletedNCT05765682

Mepivacaine Vs. Bupivacaine Spinal for TKA

Mepivacaine Vs. Bupivacaine Spinal: Effect on Return of Motor Function, Time to Ambulation, and Length of Stay in Total Knee Arthroplasty

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
160 (actual)
Sponsor
Medical University of South Carolina · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERMepivacaine Spinalspinal block using 60mg of mepivacaine
OTHERBupivacaine Spinalspinal block using 10mg of bupivacaine

Timeline

Start date
2023-03-13
Primary completion
2024-08-23
Completion
2024-08-25
First posted
2023-03-13
Last updated
2024-09-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05765682. Inclusion in this directory is not an endorsement.