drugset / Trial / NCT03476642

Distribution, Pharmacokinetics and Extent of Sensory Blockade in ESP Blocks

NCT03476642 ↗

Phase 4 Completed 12 enrolled Milton S. Hershey Medical Center
RandomizedParallel-groupQuadruple-blindBasic science

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.

Timeline

Start
2019-07-02
Primary completion
2024-02-19
Completion
2024-03-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Epinephrine Other / unclassified 20 ml —
Comparator Ropivacaine Other / unclassified 0.5 % —
Comparator Ropivacaine Other / unclassified 20 ml —

Indications

No indication recorded.