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Mepivacaine Versus Bupivacaine Onset Time in Ultrasound-guided Ankle Blocks

Foot Surgery Clinical Trial

Official title:
Onset of Sensory Blockade in Ultrasound-Guided Ankle Block With Mepivacaine Versus Bupivacaine: A Randomized Non-Inferiority Clinical Trial

Clinical Trial Summary

The purpose of this research is to determine if both local anesthetics (mepivacaine and bupivacaine) are similar in their onset of sensory block to assess the efficiency of ultrasound-guided ankle blocks in our practice. Currently it is the standard of care to perform ankles blocks with both mepivacaine and bupivacaine. However, given similarity in their safety profile researchers would like to compare if one is non-inferior to the other in terms of onset time of ankle block.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05425979
Study type Interventional
Source Mayo Clinic
Contact
Status Enrolling by invitation
Phase Phase 4
Start date March 11, 2024
Completion date December 2024
View Details
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