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Clinical Trial Summary

The purpose of this study is to determine the optimal amount of lidocaine buffering needed to decrease injection pain when administering local anesthesia.


Clinical Trial Description

Once the site is chosen, the skin will be anesthetized as usual. This study will utilize a commercially prepared 1% lidocaine solution mixed with standard sodium bicarbonate. A total of 10 mL will be used. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02647892
Study type Interventional
Source University of Nebraska
Contact
Status Terminated
Phase Phase 4
Start date January 8, 2016
Completion date November 5, 2021

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