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Clinical Trial Summary

The study is designed as a randomized parallel controlled trial with three groups. Participants aged above 18 years with the first permanent molars with symptomatic signs of irreversible pulpitis will be randomly assigned into 3 groups. The first group (experimental group) will be injected with 4% articaine 1:100.000 epinephrine (inferior alveolar nerve block) will be anesthetized using 4% articaine 1:100.000 plus cryotherapy application, and the second group (experimental group) will be anaesthetised with IANB plus buccal infiltration. For the third group (control group), the mandibular molars will be anaesthetized using epinephrine using the inferior alveolar nerve block.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05427903
Study type Interventional
Source Minia University
Contact Ahmad Elheeny, PhD
Phone 00201064257135
Email ahmedelheeny@mu.edu.eg
Status Recruiting
Phase N/A
Start date March 4, 2022
Completion date July 1, 2022

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