drugset / Trial / NCT01981772

Efficacy of Buffered Lidocaine in Patients With Facial Swelling

NCT01981772 ↗

Completed 88 enrolled Ohio State University
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine the clinical efficacy of a buffered 4% lidocaine solution for incision and drainage. Ninety patients will be examined clinically to determine a diagnosis of cellulitis or fluctuance. The diagnosis will be confirmed by incision and drainage. Patients will receive either 3.6 ml 4% lidocaine with 1:100,000 epinephrine or 3.6 ml 4% lidocaine with 1:100,000 epinephrine buffered with 8.4% sodium bicarbonate. Patients will rate pain prior to and throughout the procedure.

Timeline

Start
2013-03
Primary completion
2014-06
Completion
2014-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lidocaine Other / unclassified 4 % —
Background Epinephrine Other / unclassified — —

Indications

No indication recorded.