Other Clinical Trial - Anaesthetic Efficacy of 2% Mepivacaine Versus 4%

Status Completed

Clinical Trial Summary

Clinical Trial Description

The aim of this randomized, double-blinded, clinical trial was to assess the effect of 3.6 mL 2% mepivacaine hydrochloride with 1:100,000 epinephrine compared to 3.4 mL 4% articaine hydrochloride with 1:100,000 epinephrine on the success of the inferior alveolar nerve block for patients with symptomatic irreversible pulpitis in mandibular molars. Patients were clinically and radiographically examined and their eligibility assessed and preoperative pain was measured using the numerical rating scale (NRS). Patients were randomly assigned to one of 2 groups: experimental group (2% mepivacaine) and the control group (4% articaine). After 15 minutes of the inferior alveolar nerve block (IANB), patients reporting lip numbness had their molars accessed. No-to-mild pain response was considered success during root canal preparation. ;

Study Design

Related Conditions & MeSH terms

Pulpitis
Symptomatic Irreversible Pulpitis

Clinical Trial Details

NCT number	NCT04822415
Study type	Interventional
Source	Cairo University
Contact
Status	Completed
Phase	N/A
Start date	December 2014
Completion date	December 2016

View Details

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Anaesthetic Efficacy of 2% Mepivacaine Versus 4% Articaine With Symptomatic Irreversible Pulpitis

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms