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Clinical Trial Summary

The primary objectives of this study are to define the extent of dermatomal anesthesia and anatomical spread of injectate (as defined by MRI imaging) that is provided by an ESP block at the T5 level, using twenty milliliters of 0.5% ropivacaine. The secondary objectives include: 1) the measurement of changes in hemodynamic parameters associated with the ESP block, 2) the duration of sensory effects provided by ropivacaine with or without epinephrine, 3) the venous plasma concentration of ropivacaine associated at various time intervals after completion of the ESP block.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Distribution of Ropivacaine in Erector Spinae Plane Block

NCT number NCT03476642
Study type Interventional
Source Milton S. Hershey Medical Center
Contact
Status Completed
Phase Phase 4
Start date July 2, 2019
Completion date March 31, 2024