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Volume Increase Versus Supplemental 4% Articaine Buccal Infiltration on Mepivacaine Inferior Alveolar Nerve Block Success

Symptomatic Irreversible Pulpitis Clinical Trial

Official title:
Effect of Volume Increase Compared to Supplemental 4% Articaine Buccal Infiltration on Mepivacaine Inferior Alveolar Nerve Block Success in Cases With Symptomatic Irreversible Pulpitis: A Randomized Clinical Trial

Clinical Trial Summary

To assess the anesthetic success of inferior alveolar nerve block (IANB), intraoperative pain intensity and need for supplemental anesthesia on administration of 1.8ml or 3.6ml 2% mepivacaine IANB, or 1.8ml 2% mepivacaine IANB plus 1.8ml 4% articaine buccal infiltration (BI) in mandibular molars with symptomatic irreversible pulpitis.

Clinical Trial Description

Patients with moderate-to-severe preoperative pain related to mandibular molars with symptomatic irreversible pulpitis will be included. Patients receive 1.8 ml, 3.6 ml 2% mepivacaine IANB, or 1.8ml 2% mepivacaine IANB plus 1.8ml 4% articaine BI. Anesthetic success of inferior alveolar nerve block, intraoperative pain intensity and need for supplemental anesthesia will be assessed during treatment. ;

Study Design

Related Conditions & MeSH terms

  • Pulpitis
  • Symptomatic Irreversible Pulpitis
Clinical Trial Details
NCT number NCT05238727
Study type Interventional
Source Cairo University
Contact Reham Anwar Sleem
Phone 00201014110666
Email reham.anwar@dentistry.cu.edu.eg
Status Not yet recruiting
Phase N/A
Start date March 2022
Completion date September 2023
View Details
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