Evaluation of Buffered Local Anesthesia in Dental Extraction.

Status Not yet recruiting

Clinical Trial Summary

To compare pain during injection, onset of anesthesia and effectiveness of anesthesia using buffered versus non- buffered 2% lidocaine with 1:80,000 adrenaline in dental extraction.

Clinical Trial Description

The investigators will conduct a prospective, randomized, single-blinded study, the sample will include 100 patients (extraction) who need dental extraction of upper teeth (premolar and molar teeth). The predictor variable is the use of buffered 2% lidocaine with 1:80,000 adrenaline and non-buffered 2% lidocaine with 1:80,000 adrenaline. The patients will be randomly assigned into two groups of 50 patients each using Microsoft Excel 2016; the first group (study group) will undergo dental extraction after receiving buffered 2% lidocaine with 1:80,000 adrenaline, the second group (control group) will undergo dental extraction after receiving non-buffered 2% lidocaine with 1:80,000 adrenaline. The outcome variables include pain during injection, onset of anesthesia and effectiveness of anesthesia on buffered and non-buffered group. ;

Study Design

Related Conditions & MeSH terms

Anesthesia, Local

Clinical Trial Details

NCT number	NCT04773236
Study type	Interventional
Source	University of Baghdad
Contact
Status	Not yet recruiting
Phase	Phase 4
Start date	February 22, 2021
Completion date	August 22, 2021

View Details

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