Clinical Trials Directory

Trials / Completed

CompletedNCT02226913

Effect of Sodium Bicarbonate Buffered Lidocaine on the Success of IAN Block of Teeth With Irreversible Pulpitis

Effect of Sodium Bicarbonate Buffered Lidocaine on the Success of Inferior Alveolar Nerve Block for Teeth With Symptomatic Irreversible Pulpitis: A Prospective, Randomized Double-blind Study

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Masoud Saatchi · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Buffering of local anesthetics (alkalinization) has been suggested in achieving pain control. The purpose of this prospective, randomized, double-blind study was to evaluate the effect of adding 0.6 mL 8.4% sodium bicarbonate to 3.0 mL 2% lidocaine with 1: 80,000 epinephrine on the success rate of IAN block for endodontic treatment of mandibular molars with symptomatic irreversible pulpitis.

Detailed description

Some studies have been shown buffering of local anesthetics reduce pain of injection, hasten the onset of anesthesia, and improved success rate of anesthesia. Others reported buffering of local anesthetics cannot reduce pain of injection, hasten the onset of anesthesia, and improve success rate of anesthesia. There are no studies evaluating a sodium bicarbonate-buffered lidocaine formulation for IAN block for teeth with irreversible pulpitis.

Conditions

Interventions

TypeNameDescription
DRUG2% lidocaine with 1:80,000 epinephrine2% lidocaine with 1:80,000 epinephrine
DRUGsodium bicarbonate8.4% sodium bicarbonate
DRUGplacebosterile distilled water (Samen Pharmaceutical Co, Iran)

Timeline

Start date
2013-02-01
Primary completion
2013-09-01
Completion
2013-09-01
First posted
2014-08-27
Last updated
2016-08-31

Source: ClinicalTrials.gov record NCT02226913. Inclusion in this directory is not an endorsement.