drugset / Trial / NCT03059498

PECS Block: Plasma Bupivacaine Level

NCT03059498

Phase 0 Completed 20 enrolled Wake Forest University Health Sciences
Non-randomizedParallel-groupOpen-labelOther

Summary

The purpose of this study is to determine peak plasma bupivacaine concentrations in a similar fashion for PECS I/II blocks. The investigators hypothesis is that the mean peak plasma levels for patients undergoing PECS I/II blocks will be less than the levels reported to cause early neurotoxicity of \[2.2 (0.9) micrograms/ml\]6 in patients receiving intravenous bupivacaine infusions.

Timeline

Start
2017-06-06
Primary completion
2017-11-15
Completion
2017-11-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bupivacaine Other / unclassified 0.25 % Other
Comparator Bupivacaine Other / unclassified 30 ml Other

Indications

No indication recorded.