CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 88 enrolled
Drug / intervention
4% lidocaine with 1:100,000 epinephrine +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01981772
NCT01981772N/ACompleted
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Anesthetic Efficacy of 4% Buffered Lidocaine in Emergency Patients With Facial Swelling.

Ohio State University·interventional·Posted Nov 13, 2013·Updated Oct 12, 2020

In Brief

A clinical study evaluating 4% lidocaine with 1:100,000 epinephrine and 4% buffered lidocaine with 1:100,000 epinephrine for Orofacial Swelling. Completed, enrolled 88 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOrofacial Swelling
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedNov 13, 2013
Enrollment StartMar 1, 2013
Primary CompletionJun 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 12.6 years ago

Interventions

4% lidocaine with 1:100,000 epinephrinedrug

see arm/group description

4% buffered lidocaine with 1:100,000 epinephrinedrug

see arm/group description